2010-03-04T18:29:46-08:00 <b>Mass Spectroscopy, Scientist - Sr Scientist:</b> #2087 <b>More details/Apply:</b> http://RSABioJobs.com/JobOpenings.htm#2087 <b>Referral Program:</b> http://RSABioJobs.com/Referral.htm <b>Keywords: Mass Spec/Mass Spectrometry, LCMS, LC/MS, LC-MS;</b> (nano LCMS), Proteomics, Deamidation, Glycosylation, Chromatography, ESI LC-MS/Electrospray ionization LC MS, Post-translational changes. <b>Recombinant Proteins, Therapeutic Proteins, Monoclonal Antibodies.</b> Mass Spec position for the Analytical BioChem Development Dept – this person will be responsible for protein structure, identification and characterization. <b>CMC/Chemistry, Manufacturing & Controls</b> training/experience is required. Location: MidAtlantic States /East Coast (US) Please contact us either via our website or directly at the tel and em address below. All correspondence is kept confidential and only released with your explicit permission. -------------------------------------------------------------------------------- Ann Rathbun /(Ms) Basirah Al'Basit <b>RS&A</b> ~ Scientific Search Sedona, AZ 86341 USA <b>TEL:</b> (928) 203-0074 <b>EM:</b> RSA@RSABioJobs.com <b>Web:</b> http://RSABioJobs.com 164 MidAtlantic (US) States / East Coast RS&A ~ Scientific searches in the BioPharma/Pharma industries 2010-03-04T18:33:41-08:00 19475 2010-03-01T08:07:32-08:00 Our client, one of the world’s leading pharmaceutical companies, is currently looking for a Medical Information Advisor to join their team based in Luton in Bedfordshire, UK. Working as a Medical Information Advisor you will provide a high quality, comprehensive, technical and scientific information service for external customers on the product range, supporting and enhancing the safe and effective use of products, enabling customers to make informed decisions about the product range. Further responsibilities of this Medical Information Advisor role will include: • Provide a first line technical and scientific information service to external customers in line with company and industry standards • Liaise with the European Medical Information Advisers or Medical Affairs Scientists on enquiries requiring specialist support • To be aware of and pass on product and issue focused commercial feedback on products to key internal groups. • Ensure Medical Information activities are in line and comply with the ABPI Code of Practice. • Responsible for handling all enquiries, in particular adverse event reports and pregnancy reports, in line with local and global procedures and systems. • Responsible for the management of Product Quality complaints in line with local and global procedures and systems (GCM) and highlight major quality incidents to the Head of Regulatory Affairs and Medical Information & Patient Safety Manager. • Partake in project work as directed by Medical Information & Patient Safety Manager. The successful applicant for this Medical Information Advisor role will have a Life Sciences Degree and will have experience of working in the pharmaceutical or healthcare industry in a Medical Information role. You will be an effective communicator and be able to work on your own initiative as well as being part of a cross functional team. This is a fantastic opportunity for the right candidate to develop their career with one of the world’s leading pharmaceutical companies. If you would like more information about this Medical Information Advisor role, please contact Hendre Moolman on 01438 743 047 or email hmoolman@ckclinical.co.uk. About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical 163 Luton, Bedfordshire CK Clinical 2010-03-01T08:07:32-08:00 19267 2010-02-25T21:20:56-08:00 1) Experience in using molecular modeling and simulation software and techniques such as protein – ligand docking, QSAR, virtual library generation, pharmacophore based drug design etc. for new molecule design; excellent grasp of such software and their applications 2) Prospect and interact with lead prospects for technology demonstration, techno commercial discussions and sales closing 3) Pro-actively identify, maintain and grow customer accounts by understanding customer's needs, meeting sales targets and using internal resources to effectively execute timely solutions 4) Organize and conduct training, technical, sales visits or online sessions for the purpose of helping customers understand the technology products 5) Act as a strong support person for the software and services 6) Provide recommendations to the sales and technology teams that will have a positive impact on sales 7) Attend and present technology at relevant conferences, technical and trade meets 162 USA ABLE C DRIVE 2010-03-03T03:03:13-08:00 19460 2010-02-25T12:36:35-08:00 Below are the required details: 6 month contract with a possible extension to 1 year. Department Epidemiology Job Code Manager, Med Affairs Job Title Principal Patient Reported Outcomes Duties To maximize the value of multiple agents within a therapeutic area by developing Patient Reported Outcome (PRO) strategies during early clinical development. The inclusion of PRO measures in trials is critical for creating robust and differentiated product profiles and for providing information important for therapeutic decision-making to patients, physicians and payers. Job Description Lead Patient Reported Outcome activities for a therapeutic area and develop global PRO strategies for molecules within a therapeutic area. Responsibilities oWork cross-functionally with Global Development, Global Product Strategy, International Business Teams, Global Health Economics and Affiliates to develop PRO strategies oEnsure relevant PRO endpoints and study design for registration clinical trial programs meet the needs of global regulatory agencies and key stakeholders oIdentify PRO instruments and evaluate measurement and psychometric properties of the instruments oWork with external key opinion leaders and regulatory agencies to obtain guidance on PRO strategies oContribute to the design, implementation, and management of registration clinical trials containing PROs including the development of the PRO sections of study concept documents, study protocols, statistical analysis plans, clinical study reports and other development documents oDevelop and/or validate instruments for PRO as needed oAdapt and validate instruments for use in different patient populations, including cultural adaptations and translations oWork with Global Scientific Communications to develop publication plan that is integrated with overall publication strategy to communicate PRO information to physicians, patients, payers, and policy makers oResponsible for Vendor management including scope of work development, contract initiation, and project milestones, timelines, deliverables, and budgets Skills Job Qualifications o Advanced degree in psychology, epidemiology, health services research, outcomes research or related discipline preferred with at least five (5) years professional experience in PRO assessment and/or psychometric validation. oFamiliarity and experience with the development and implementation of research strategies (including PRO within registration clinical trials). o Strong understanding of research methodology and statistics, as well as demonstrated technical writing and presentation skills. oExperience managing complex projects with external vendors under short timelines. oDemonstrated ability to set clear priorities in managing projects. oExperience working with key opinion leaders and regulatory agencies to inform the development of patient reported outcome strategy preferred. oProfessional experience across multiple therapeutic areas, with experience in the biotechnology or pharmaceutical industry preferred. oStrong oral and written communication skills, with the ability to communicate effectively to internal and external audiences. oAbility to work effectively in a cross-functional, project team environment. Please send in your resumes to tpriyanka@idexcel.com. Awaiting apt resume!!!:) Regards, Priyanka 161 San Francisco, CA IDEXCEL Inc 2010-02-25T12:36:35-08:00 19325 2010-02-25T12:32:33-08:00 Below are the details: Duration: 6 month contract with a possible extension to 1 year. Job Category : Drug Devt - Med/Clin Affairs Job Title: Clinical Safety Assoc II Duties Purpose: The Clinical Safety Associate II (CSA II) assists in the clinical processing of adverse event (AE) information received by(GDS). Responsibilities are performed under the direction of the Manager, Case Management. Skills ,Essential Functions/Responsibilities: * Demonstrates advanced knowledge of safety concepts, focused on standards set out in ICH and FDA guidelines for drug safety reporting requirements and applies them in daily activities. * Performs data entry and coding for all molecules. * Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for incorporation into the case narrative. Education : Experience/Knowledge/Skills: * RN, BSN, PA, NP, MSN, MD, or PharmD required * Minimum 2 years of clinical experience in a health care related field * Minimum 2 years of previous experience in Drug Safety required * Computer proficiency and data entry experience preferred * Excellent communication skills, both written and verbal * Previous experience in Drug Safety (preferred) Please let me know if there are any further questions. Send in your resume to tpriyanka@idexcel.com. Awaiting resumes!!!!!!!!!:) Have a great day!!! 160 San Francisco, CA IDEXCEL Inc 2010-02-25T12:39:34-08:00 19325 2010-02-25T09:18:43-08:00 • Contract position • Upwards of £400 per day • Cambridgeshire or Middlesex • Global Biotech company A global biotech company require a number Clinical Study Managers to work in their Cambridgeshire or Middlesex offices. These are regional Clinical Study Manager roles are based at a Global Development centre but may be assigned Global responsibility as the Lead CRSM on a given study. There are vacancies available in the Oncology, Inflammation, Bone and Nephrology therapy areas. Reporting to the Clinical Research Programme Manager, you will be responsible for the following: • The planning, management and reporting of clinical studies conducted by Development through oversight of cross-functional study activities; identification and resolution of issues; and communication of study timelines / deliverables • Ensuring implementation of study(ies) in accordance with SOPs and ICH / GCP guidelines • Contributing to the Global Development Plan • Contributing to /authoring study concept documents, protocols, clinical study reports, and publications • Management of study budget, timelines and insourcing/outsourcing partners to the required standards • May have line-management responsibilities of Clinical Trial Specialists Mentoring / training and career development of staff (where relevant) These are exciting global roles, you will join a team at the core of the business, with plenty of scope to make your mark and develop your career. For further details please contact Jim Gleeson on Tel: +44 (0)1438 870027 who specialises in this field. Email: jgleeson@ckclinical.co.uk Alternatively, click here to apply for this Clinical Study Manager job now. http://ckclinical.co.uk/job/Clinical-Research-Study-Manager/294cafd92fP4KO About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical 159 Cambridgeshire and Middlesex CK Clinical 2010-02-25T09:19:08-08:00 19267 2010-02-25T02:09:10-08:00 CK Clinical is proud to be working on a new opportunity with a rapidly expanding Global pharmaceutical company. This is a high profile position in which you will oversee and manage global or regional development programs or multiple multinational phase II/III clinical trials in order to achieve a high quality product for the marketplace and business success for the organisation. As the Director of Clinical Development you will be the point of contact for interactions with regulatory-agency clinical reviewing divisions on clinical matters, oversee management and performance of CROs and ensure high quality products for the business. The successful individual must be educated to MD or DPharm level with demonstrable hands on experience leading a multi-country, oncology clinical program. This is a very rare opportunity to join an expanding global pharmaceutical company and to take your career to the next level. If you are interested in finding out more about this Director of Clinical Development role please contact Ben Traies at CK Clinical on 01438 743047 or email btraies@ckmedics.com Alternatively, click here to apply for this Director of Clinical Development job now: http://ckclinical.co.uk/job/Director-Of-Clinical-Development/90b7fd373GIBP About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical 158 London, Greater London, UK CK Clinical 2010-02-25T02:09:10-08:00 19267 2010-02-23T15:20:18-08:00 Description NMR Scientists! Want to upgrade your job..and company? If you are a "hardware junkie" and love to tinker with the NMR hardware this unique job may be for you! If you have found yourself hand-building your own nifty NMR probes, you can move to a great job with a very trusted and successful instrument manufacturer in the SFO Bay area. This is a job with variety including design, build, research and "detective work". This is a non-contract position and includes competitive salary and a full benefit package. US Citizens or US Permanent Residents only. I have placed great engineering candidates at this company for nearly 9 years. For more details please contact me or send your resume to me at:minda@informativepeople.com, or 925-833-8714x160. 157 San Francisco Bay Area, California Informative People Inc. 2010-02-23T15:20:18-08:00 18616 2010-02-23T06:06:50-08:00 • Contract Position • Very good salary bonus and benefits Due to continued growth and success, a leading global pharmaceutical company with offices in Hertfordshire, are looking for a Senior Medical Advisor to join their team on a contract basis. Working as a Senior Medical Advisor you will provide support for two marketed products in the critical care franchise, and the pre-launch activity for a phase III compound in severe sepsis. Based at the companies European Headquarters you will work in collaboration with Global Medical Marketing services to tailor global launch plans for the European region. You will define and implement European Key Opinion Leader strategy, and collaborate with Global Health Economics and Outcomes Research to maximise European market access and reimbursement. In addition to this you will have functional management of a medical affairs scientific advisor. The ideal candidate for this Senior Medical Advisor role will be GMC registered with a solid and extensive prior experience in a Medical Affairs role. Experience in critical care is also essential. You will have good business/commercial acumen with effective communication skills and a desire to succeed in a commercial environment. If you are interested in finding out more about this exciting role please call Ben Traies on 01438 870021 or email btraies@ckmedics.com Alternatively, click here to apply for this Senior Medical Manager job. About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical 156 Hertfordshire, UK CK Clinical 2010-02-23T06:07:43-08:00 19267 2010-02-23T06:05:41-08:00 • Permanent Position • Very good salary bonus and benefits Due to continued growth and success, a leading global pharmaceutical company with offices in Hertfordshire, are looking for a Senior Medical Advisor to join their team on a permanent basis. Working as a Senior Medical Advisor you will provide support for two marketed products in the critical care franchise, and the pre-launch activity for a phase III compound in severe sepsis. Based at the companies European Headquarters you will work in collaboration with Global Medical Marketing services to tailor global launch plans for the European region. You will define and implement European Key Opinion Leader strategy, and collaborate with Global Health Economics and Outcomes Research to maximise European market access and reimbursement. In addition to this you will have functional management of a medical affairs scientific advisor. The ideal candidate for this Senior Medical Advisor role will be GMC registered with a solid and extensive prior experience in a Medical Affairs role. Experience in critical care is also essential. You will have good business/commercial acumen with effective communication skills and a desire to succeed in a commercial environment. If you are interested in finding out more about this exciting role please call Ben Traies on 01438 870021 or email btraies@ckmedics.com Alternatively, click here to apply for this Senior Medical Manager job. About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical 155 Hertfordshire, UK CK Clinical 2010-02-23T06:05:41-08:00 19267 2010-02-23T04:57:01-08:00 CK Clinical is proud to be working with one of the leading healthcare companies in the UK. In this exciting new role of Medical Science Manager you will ensure that the UK has a high quality scientific information services. Working as a Medical Science Manager you will lead and manage a team of high calibre information scientists to set up and develop an information system, which will form the basis for the Company to offer healthcare advice to consumer and customers; as well as medical input to marketing campaign. Further responsibilities of this Medical Science Manager job will include: • To lead the continuing development of the joint relationship with the UK Marketing Department to ensure highest quality of scientific content in marketing campaigns • To establish and manage excellent, productive relationships with external professional bodies such as BNF and Royal Pharmaceutical Society • To support the UK Medical Director in building relationships with key opinion leaders in clinical focus areas including pain management, gastroenterology and other areas related to marketed products. • To ensure the successful operation of the copy approval process using internal electronic systems and in line with standard operating procedures • To train others in the provision of excellent services for compliance • To ensure a successful collaborative approach between all stakeholders in the approval process for communication and to achieve compliance in all cases • To provide support for pharmacovigilance team within medical department as needed If you are interested in this exciting new Medical Science Manager opportunity please contact Ben Traies on 01438 870021 or email btriaes@ckmedics.com Alternatively, click here to apply for this Medical Science Manager job now: http://ckclinical.co.uk/job/Medical-Science-Manager/f4e757d5GJKO About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical 154 Slough, UK CK Clinical 2010-02-23T04:57:01-08:00 19267 2010-02-23T02:29:39-08:00 Our client, one of the world’s leading pharmaceutical companies is currently looking for an EU Regulatory Strategist to join their team based in the South of England. Reporting to the EU Regulatory Strategy Portfolio Manager, your role will include: • Ensuring EU contribution to Global Regulatory Strategies and implementation plans. • Ensuring that the regulatory contributions work towards achieving the objectives in the strategy. • Be responsible for providing the required regulatory contributions to project teams, adhering to time and cost deadlines. • To liaise with Senior Management regarding regulatory plans. • Work closely with the Regulatory Product manager to ensure consistent and appropriate process, working practices and quality standards. The ideal candidate for this EU Regulatory Strategist role will be educated to a minimum degree level in a scientific subject and will have demonstrable have experience of the following: • EU regulations. • CTA and MAA submissions process. • Management of complex regulatory issues. If you would like to hear more about this EU Regulatory Strategist job, please contact Meera Pattni on 01438 743047 or email mpattni@ckclinical.co.uk. Alternatively, click here to apply for this EU Regulatory Strategist job : http://regaffairsjob.com/job/EU-Regulatory-Strategist/efa148921IJKO Click here to search for other Regulatory Affairs jobs: http://regaffairsjob.com/search/regulatory About CK Regulatory CK Regulatory is a specialist Recruitment company offering job opportunities to Regulatory Affairs professionals seeking work in Pharma, Biotechnology, Medical Devices and Regulatory Consultancies. As part of CK Clinical we have an established and enviable track record of providing a high quality recruitment service to Pharmaceutical professionals. - Visit the CK Regulatory website: http://regaffairsjob.com/ - Join us on Linkedin: http://www.linkedin.com/groups?about=&gid=2362708&trk=anet_ug_grppro - Follow us on Twitter: http://twitter.com/ckregulatory/ 153 South of England CK Regulatory 2010-02-23T02:29:39-08:00 19267 2010-02-18T02:30:13-08:00 Our client is currently seeking to recruit an experienced Biomedical Scientist with extensive Transfusion and/or Transplantation knowledge to work with them on an ongoing locum basis to cover long term sick leave. This Biomedical Scientist role will involve performing, analysing, interpreting, documenting and reporting routine and complex investigations in any diagnostic laboratory e.g. Red Cell, Immunohaematology, histocompatibility and immunogenetics, reference microbiology, donation testing or research. You will also be involved in leading and mentoring other staff members. The successful candidate for this Biomedical Scientist role Candidates will be a registered Biomedical Scientist and will also be HPC registered. Candidates must also have experience within Transfusion and or Transplantation laboratory. Candidates must be eligible to work in the EEA. If you would like more information about this Biomedical Scientist role, please contact Philippa Robertson on 0114 2839956 or email probertson@ckscience.co.uk. Please quote HC19265 in all correspondences. About CK Healthcare CK Healthcare is the new name in healthcare recruitment, specialising in the recruitment of locum Allied Health Professionals and Health Service Scientists to the NHS. Our team of specialist recruiters are here to help you achieve your career ambitions within the scientific industry. We actively offer you careers advice, help with writing your CV, assistance with interview preparation and up-to-date information about the industry. We pride ourselves on providing an honest, straight-forward and trustworthy service to both our clients and candidates. • Visit our website: http://ckhealthcare.com/ • Join our Linkedin group: http://www.linkedin.com/groups?about=&gid=2148811&trk=anet_ug_grppro • Meet the team on Youtube: http://www.youtube.com/ckhealthcare • Follow us on Twitter: http://twitter.com/ckhealthcare Keywords: Healthcare jobs, Biomedical scientist, HPC registered, Transfusion, Transplantation, blood, immunohaematology, histocompatability, immunogenetics, scientific recruitment, science jobs, jobs in science, scientist jobs, north east, uk, healthcare recruitment, healthcare jobs, locum work, locum jobs. 152 North East, UK CK Healthcare 2010-02-18T02:30:13-08:00 19267 2010-02-17T14:06:07-08:00 NMR engineers! Want to upgrade your job..and company? Use your NMR probe design and build background to move to a very trusted and successful instrument manufacturer in the SFO Bay area. If you have designed RF coil circuits and enjoy a job with variety including design, build, research and "detective work", this may be for you! This is a non-contract position and includes competitive salary and a full benefit package including relocation assistance from other US areas. I have placed great engineering candidates at this company for nearly 9 years. For more details please contact me or send your resume to me at:minda@informativepeople.com, or 925-833-8714x160. 151 San Francisco California Informative People Inc. 2010-02-17T14:06:07-08:00 18616 2010-02-17T14:03:55-08:00 Use your FTIR and/or UV Vis sales experience to move to a successful, customer-focused company. You'll sell trusted equipment, and team up with an experienced sales manager. Based in Kansas City or St Louis area, cover central US. If you'd like to hear more, please contact me directly at: minda@informativepeople.com 925-833-8714x160 150 Missouri; territory to cover Central US Informative People Inc. 2010-02-17T14:03:55-08:00 18616 2010-02-17T14:01:31-08:00 Use your single-crystal experience and professional contacts in a job with lots of travel and variety! You’ll be the “technical expert” in Eastern US for trusted X-ray crystallography products; provide technical pre and post sales support. Take care of major accounts. Use your contacts to “spread the word” about our wonderful instruments and generate sales leads. Close some sales of your own. This one’s for a crystallography expert; a “road warrior” with lots of great contacts living in Eastern US near a major airport. You will cover Eastern US to Chicago; your home base is flexible. Compensation to 150K, VERY good "upside potential". Please feel free to call me today, at 925-833-8714x160, or send resume to me: minda@informativepeople.com. Thanks! 149 Eastern US, near a major airport Informative People Inc. 2010-02-17T14:35:35-08:00 18616 2010-02-16T09:40:33-08:00 PRODUCT MANGER II, MULTIPLEXING AND IMMUNOASSAYS, Protein Research Assays Group SUMMARY The Biomarkers and Immunoassays (BMIA) marketing group is in the Drug Discovery strategic business unit at Millipore and is responsible for a portfolio of products and services focused on immunodetection assays for ELISAs, RIAs, and multiplexing using the Luminex xMAP® technology with major focus on assays for metabolic diseases, inflammation and cell signaling. The successful candidate will assist in the development and implementation of marketing for products and services within the BMIA segment. The primary responsibilities will include executing product line strategies and plans, developing marketing communication materials, and technical training of sales force. RESPONSIBILITIES Develop a business plan and marketing strategies to assist in selling immunoassay products for ELISA and multiplexing assays. Develop and implement strategy, commercialization and marketing plan for immunoassay portfolio emphasizing technical expertise in the areas of protein detection and neuroscience applications. Oversee product lifecycle management, price optimization and new product development. Provide product support and develop a technical training program to support the global sales staff. Support marketing communications to develop print and electronic collateral. Define market needs and direction, identify opportunities for new products and process solutions. Attend key scientific/industry meetings to evaluate advancements in the drug discovery process. Gather, collate, analyze, and disseminate market information relating to trends, size, technology, competitors, and pricing. Attend scientific meetings as a representative of the multiplexing/immunoassay group at the Millipore sponsored exhibits. Collaborate with R&D and technology transfer teams to execute the launch of new products. Provide technical training and updated market assessments for the sales force. Maintain databases for sales tools and product information. Interface with technical support, R&D, and manufacturing for maintaining product performance and quality. QUALIFICATIONS An advanced degree in a scientific discipline with at least 2-3 years of product management for immunoassay products. Technical knowledge and laboratory experience and expertise in immunodetection assays and/or biomarkers and multiplexing technologies with a particular emphasis in neuroscience applications. Strong analytical skills with proven excel proficiency and the ability to organize and interpret complex data sets. Self-starter and strategic thinker with the ability to work quickly in a fast-paced environment Advanced technical writing skills with experience in developing marketing pieces that target scientific community Must be able to present ideas in a clear, organized fashion, both orally and in writing. Ability to travel domestically and/or internationally. Travel may be approximately 25%. 148 St. Charles, MO Millipore 2010-02-16T09:40:33-08:00 19431 2010-02-15T08:50:18-08:00 Our client, one of the largest and most well established pharmaceutical companies in the world, are currently looking for a Regulatory Affairs Specialist to join their team based in Basel, Switzerland. Working as a Regulatory Affairs Specialist, you will provide Regulatory support to the company in order to obtain Marketing Authorisations for commercial products as rapidly as possible and to maintain these authorisations and provide input into all stages of development and develop strategies to ensure a complete and rapid development. Reporting to the Regulatory Affairs Manager or Head of Franchise, the main activities involved with this Regulatory Affairs Specialist job include the following: • Prepare, coordinate and having responsibility for the preparation of regulatory submissions such as clinical trials applications, variations, renewals, support for marketing applications etc. (under the general guidance of their supervisor). • Participate in the approval of promotional material as required and helping to resolve external medical/technical enquiries, when required. • Sit on designated working teams and providing regulatory input to these teams including preparation of draft position papers on regulatory issues, draft regulatory sections of project plans and to develop regulatory strategies. • Aid in the maintenance of the departmental archive of administrative and technical documentation according to internal procedure. The successful candidate for this position will be educated to a minimum degree level in a relevant field of expertise, along with 2-3 years work experience within Pharmaceutical Regulatory Affairs. In addition to this, the following skills and competencies are required for this Regulatory Affairs Specialist job: • Knowledge of regulatory procedures and requirements. • Working knowledge of electronic tools/systems. • Advanced level in both written and oral English. • Ability to work in an autonomous manner and manage his/her time. • Good communication skills and culturally aware. • Experience in participating in Cross-Functional teams If you would like to hear more about this Regulatory Affairs job, please contact Jonathan Hart-Smith on 01438 743046 or email jhartsmith@ckclinical.co.uk. Apply for this Regulatory Affairs Specialist job now: http://ckclinical.co.uk/job/Regulatory-Affairs-Specialist/6db8e70827IQKO About CK Regulatory CK Regulatory is a specialist Recruitment company offering job opportunities to Regulatory Affairs professionals seeking work in Pharma, Biotechnology, Medical Devices and Regulatory Consultancies. As part of CK Clinical we have an established and enviable track record of providing a high quality recruitment service to Pharmaceutical professionals. • Visit the CK Regulatory website: http://regaffairsjob.com/ • Join us on Linkedin: http://www.linkedin.com/groups?about=&gid=2362708&trk=anet_ug_grppro • Follow us on Twitter: http://twitter.com/ckregulatory/ Keywords: regulatory affairs specialist jobs, regulatory affairs jobs, reg affairs, job, jobs, uk, basel, Europe, Switzerland, reg affairs recruitment, pharmaceutical regulatory affairs, ck regulatory. 147 Basel, Switzerland CK Clinical 2010-02-15T08:50:18-08:00 19267 2010-02-15T04:54:38-08:00 A Worldwide Pharmaceutical company with offices in Belgium are looking for an experienced Clinical Data Project Manager to join their team. If you are an experienced Data Manager that is looking to explore new cultures, whilst working in a challenging and stimulating environment this might just be the role for you. In this role you will manage outsourced studies in EDC from set-up to Data base lock, providing Data Management support for Clinical Databases with limited supervision. Further key responsibilities of this Clinical Data Project Manager job will include: • To manage projects according to strict timelines. • To manage 'end to end' process of outsourced studies. • To maintain internal database standards for data reporting in collaboration with CDISC. • To specify the study structure and validation according to protocol specifications. • To design and study specific eCRFs • To produce, co-ordinate and perform user acceptance testing • To perform data validation • To perform SAE reconciliation where necessary • To manage and monitor change requests to eCRF and external databases • To develop and maintain working practices • To participate in Computer Systems Validation of in-house technologies • To maintain study documentation • To be the main liaison for all CRO/EDC vendors Essential Key Requirements • Several years experience in Clinical Data Management within the pharmaceutical industry • Sound knowledge of the drug development process, Data Management process and medical terminology • Clean, quality data for statistical reporting Main Demands • Ensuring work is compliant with ICH GCP and regulatory requirements • Ensuring compliance with 21 CFR Part 11 Electronic Records; Electronic signatures If yourself or anyone you know might be interested in working in this interesting and challenging position please contact Sarah Brunnen on 01438 743047, or email sbrunnen@ckclinical.co.uk. Apply for this Clinical Data Project Manager job now: http://ckclinical.co.uk/job/Contract-Clinical-Data-Manager/4f4707862eGWKO About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical Keywords: clinical data project manager jobs, data management jobs, EDC, data manager, pharmaceutical recruitment, pharmaceutical jobs, job, jobs, clinical, CRO, clinical databases, Belgium, EU, data management recruitment, ck clinical 146 Belgium CK Clinical 2010-02-15T04:54:38-08:00 19267 2010-02-15T04:00:08-08:00 Our client, a top pharmaceutical company, are currently looking for a Drug Safety Associate to join their team based in Buckinghamshire. As a Drug Safety Associate, you will be responsible for the receipt and data entry of adverse event reports following Company Standard Operating Procedures, internal business practices and regulatory guidance documents to ensure compliance with worldwide safety regulations and corporate policies. Previous case processing experience is required. Further key responsibilities of this Drug Safety Associate role will include: • Triage of incoming cases to determine seriousness for prioritisation of daily workflow. • Confirmation of Safety Co-ordinator case registry data. • Database searches as necessary. • Completion of literature searches as necessary. • Completion of remaining case data entry, including narrative or auto-narrative. • Completion of risk and quality (label, approval, manual coding & quality review steps. • Clarification of unclear or illegible information from the LSO or Call Centre. • Discuss source documents, coding conventions and ad-hoc queries with Medical Assessment Physician. • Completion of protocol request forms as necessary. • Preparation of deviation memo as necessary. • Request deletions as necessary. • Single case unblinding. • Understand relevant safety implications regarding contracts with operating companies and/or marketing partners. • Review and make suggestions for system and procedure enhancements. • Participation in inspections and audits, as required . • Participation in local or global project team. This Drug Safety Associate position will focus on working on an oncology drug, therefore experience in oncology and the Argus database is a desirable. The ideal candidate for this position will also have a Life Science degree or be a qualified nurse. Pharmacists are not suited unless they have recent experience in Drug Safety. The successful candidate will enjoy the benefits of working to a global pharmaceutical company, including a competitive rate. If you would like more information regarding this Drug Safety Associate job, please contact Hendre on Hendre on Tel: +44 (0)1438 870 023 or email hmoolman@ckclinical.co.uk quoting 19282 to indicate your interest. Apply for this Drug Safety Associate job now: http://ckclinical.co.uk/job/UK-Drug-Safety-Associate/6c3ad2b72aPQKO About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical Keywords: Drug Safety Officer, Pharmacovigilance Officer, Drug Safety Associate, Pharmacovigilance Associate, Contract, Argus, Life Science, Literature, Case processing, ck clinical, clinical jobs, pharmaceutical recruitment, pharmaceutical jobs, Buckinghamshire, uk, drug safety jobs, drug safety associate jobs, pharmacovigilance jobs. 145 Buckinghamshire, UK CK Clinical 2010-02-15T04:00:08-08:00 19267 2010-02-11T23:40:22-08:00 One of India's most promising companies in the Insilico Drug Discovery space is looking for a seasoned Application Specialist, who can help them have a strong entry into the US market. The Application Specialist's role combines deep Scientific expertise with strong Customer Management and Technology skills. The ideal person must have the following capabilities: Qualification: PhD in computational chemistry, computational biology, bioinformatics or a related field. Technical: Experience in using molecular modeling and simulation software and techniques such as protein – ligand docking, QSAR, virtual library generation, pharmacophore based drug design etc. for new molecule design; excellent grasp of such software and their applications Soft skills: Excellent oral and written communication skills, ability to work independently or with minimal oversight, confident of interacting with mid to senior level research scientists and academic faculty at customer or prospective customer sites Role Description: 1. Prospect and interact with lead prospects for technology demonstration, techno commercial discussions and sales closing 2. Pro-actively identify, maintain and grow customer accounts by understanding customer's needs, meeting sales targets and using internal resources to effectively execute timely solutions 3. Organize and conduct training, technical, sales visits or online sessions for the purpose of helping customers understand the technology products 4. Act as a strong support person for the software and services Provide recommendations to the sales and technology teams that will have a positive impact on sales 5. Attend and present technology at relevant conferences, technical and trade meets. Citizenship: A US Citizen is preferred for this role. The individual will begin as a Full Time Consultant on a monthly retainer fee + performance based incentives. The contract would be an annual contract renewable at the end of each year. Contact: Send an email to shyam@cdrivecareers.com or call on +91-9845094699 for clarifications/discussion. 144 US (person can be based anywhere in the US) One of India's fastest growing Insilico Drug Discovery Companies 2010-02-11T23:41:29-08:00 18688 2010-02-11T17:02:01-08:00 Would you love to be part of the world of CSI? Then this could be the job for you. This position is responsible for planning and executing product strategy, merchandising, sales support, and program management for our growing Genetic Identity product portfolio. Successful candidates will have: • An inherent curiosity and sincere interest in helping crime labs around the globe improve and advance the technology used for human identification via DNA and RNA • An MBA or equivalent business and marketing training experience and an M.S. or Ph.D. in life sciences with concentrated training in Biochemistry or Molecular Biology • Strong portfolio management and / or proven product or marketing management experience in molecular biology reagents and analytical instruments • Strong experience in managing products throughout the product life cycle • Experience with global product launch, positioning, and promotion • An in depth understanding of marketing functions including strategic and tactical planning and execution, marketing communications, market research, product management, distribution channels, competitive intelligence, and customer relationship management • Excellent public speaking skills to represent Promega at external meetings, conferences, and organizations and the ability to present high level information to multiple audiences based on analysis and facts • The ability to effectively develop trust, respect, and cooperation across all areas of the organization and staff levels and the ability to lead cross-functional teams • Willingness and enthusiasm to travel globally as needed Promega Corporation is an internationally recognized leader in the biotechnology industry with a strong emphasis on work-life balance. At Promega you will find a campus like setting with a casual, highly productive and professional atmosphere. Click on the link below to apply for this position. Only applications through our website will be considered for this position. https://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.jobinfo&id=23&jobid=216617&company_id=15945&version=2 Promega Corporation is an equal opportunity/affirmative action employer. Visit www.promega.com to learn more about our company. 143 Madison, WI Promega Corporation 2010-02-11T17:02:01-08:00 19411 2010-02-03T05:22:36-08:00 Our client is a leading healthcare pharmaceutical company, who specialise in the discovery and development of innovative therapies that contribute to the health and well-being of people the world over. This multinational pharmaceutical organization are currently looking for a Regulatory Submissions Manager to join their Regulatory Affairs team based in the South East of England. Reporting to the Senior Manager, Global Regulatory Operations, you will be responsible for developing the submission timelines with the team leader and eDocumentatin representative. You will be required to collect status updates from members of other teams and informing the Project manager of these activities. You will also be responsible training new members of staff on the submission process. Further key tasks involved with this Regulatory Submissions Manager job will include: • Arranging the submission team meetings. • Developing agenda items by working alongside the RA team leader. • Facilitating EU RA meetings to manage eCTD marketed product lifecycle. • Liaising with other team members regarding strategies and targets. • Developing the submission timeline. • Maintaining regulatory submissions calendar. The successful candidate for this Regulatory Submissions Manager job will have a sound knowledge of regulatory submissions/ePublishing, as well as the ability to ensure that submissions adhere to internal SOPs. Further competencies required for this job include: • Excellent communication skills to interact with colleagues. • Good problem solving skills. • Project management experience. This is an excellent opportunity for the right candidate to develop their career within Regulatory Affairs within a fast paced and nurturing pharmaceutical company which operates on a global basis. If you would like to hear more about this Regulatory Submissions Manager job, please contact Meera Pattni on 01438 743037 or email mpattni@ckclinical.co.uk. Alternatively, apply for this Regulatory Submissions Manager online now: http://regaffairsjob.com/job/Regulatory-Submissions-Manager/5faeda9bLFLO About CK Regulatory CK Regulatory is a specialist Recruitment company offering job opportunities to Regulatory Affairs professionals seeking work in Pharma, Biotechnology, Medical Devices and Regulatory Consultancies. As part of CK Clinical we have an established and enviable track record of providing a high quality recruitment service to Pharmaceutical professionals. • Visit the CK Regulatory website: http://regaffairsjob.com/ • Join our Linkedin group: http://www.linkedin.com/groups?about=&gid=2362708&trk=anet_ug_grppro • Follow us on Twitter: http://twitter.com/ckregulatory/ 142 South East, London, Home Counties CK Clinical 2010-02-03T05:22:36-08:00 19267 2010-02-03T03:51:07-08:00 View our Youtube video for this Immunoassay Development Scientist job here: http://www.youtube.com/v/J2mOozrtHxc Our client is involved in supporting healthcare providers and the pharmaceutical and biotechnology industries with technically advanced testing services. This innovative and dynamic company are currently looking for a “hands on” Immunoassay Development Scientist to join their team based in Suffolk, who is capable of developing new assays from concept through to validation and transfer to manufacturing. Reporting to the Head of Immunodiagnostics Development, you will be involved in the design and development of In-vitrodiagnostic devises using immunodiagnostic procedures. Working as an Immunoassay Development Scientist, you will oversee the maintenance and growth of hybridomas for monoclonal antibody production and the purification of component materials from sources such as recombinant organisms, hybrodomas or other biological systems. You will also assist in the design, development and troubleshooting of all immunoassay development projects to verify and validate the product. The successful candidate for this Immunoassay Development Scientist job will be educated to degree level or equivalent in a science related subject and that you have knowledge of working to GLP. Experience of analytical techniques such as ELISA, 2D electrophoresis, protein purification and cell culture is also essential. If you would like to hear more about this Scientist job, please contact Lucy Campbell on 01438 723 500 or email lcampbell@ckscience.co.uk. Please quote reference ST19177 in all correspondence. Apply for this Immunoassay Development Scientist job now: http://ckscience.co.uk/job/Immunoassay-Development-Scientist-Biotechnology/646ac3a22KFLO If you are successful after the first round of screening we will contact you within 5 working days. Entitlement to work in the EEA is essential. About CK Science CK Science is the largest independent scientific recruitment company in the UK. Our team ofspecialist recruiters are here to help you achieve your career ambitions within the scientific industry. We actively offer you careers advice, help with writing your CV, assistance with interview preparation and up-to-date information about the industry. We pride ourselves on providing an honest, straight-forward and trustworthy service to both our clients and candidates. • Visit our website: http://ckscience.co.uk/ • Follow CK Science on Twitter: http://twitter.com/cksciencejobs • Join the CK Science Linkedin group at: http://www.linkedin.com/groups?about=&gid=2118950&trk=anet_ug_grppro • Become a fan of CK Science on Facebook: http://www.facebook.com/pages/Stevenage-United-Kingdom/CK-Clinical-Ltd/102844394098?ref=nf#/pages/CK-Science/125849941618?ref=ts • Meet our team on our Youtube Channel: http://youtube.com/cksciencejobs/ Keywords: ELISA, immunoassay, assay development, 2D electrophoresis, biotechnology, Immunoassay Development Scientist, jobs, scientist jobs, immunodiagnostic procedures, science jobs, jobs in science, scientific recruitment, biotechnology jobs. 141 Suffolk, UK CK Clinical 2010-02-03T03:51:07-08:00 19267 2010-02-01T03:47:09-08:00 Our client, an independent project development consultancy serving the Upstream, Midstream and Downstream sectors, are currently looking for a Process Engineer with experience from the refinery, oil & gas or petrochemicals industry, to join their team on a contract basis. The ideal candidate for this Process Engineer job will have industrial experience in the oil & gas sector and will have worked as a Process or Project Engineer dealing with large scale design projects or have worked in a process engineering support role. It is essential you are immediately available for appointment or available at short notice to start in this role.Entitlement to work in the EEA is also essential. To hear more about this Process Engineer job, please contact Russell at CK Science on 0114 2839956 or email roakley@ckscience.co.uk. Please quote reference SH19189 in all correspondence. Apply for this Process Engineer job online now: http://ckscience.co.uk/job/Process-Engineer-Oil-Gas/fc17c822dODLO 140 London, UK CK Clinical 2010-02-01T03:47:09-08:00 19267 2010-02-01T03:45:22-08:00 Our client, a Manufacturing Laboratory dealing with blood and blood components are currently looking for a Manufacturing Shift Supervisor to join their team based in North London on a 6 month contract basis. Working as a Manufacturing Shift Supervisor, you will supervise a team of more junior staff whilst having some hands on responsibility yourself. Some understanding of blood and blood components either from working in a blood transfusion service of hospital is essential, along with supervisory experience. The facility operates a rolling shift system - 7am - 3pm and 3pm - 11pm, some weekend working will also be required. The contract is likely to be 6 months + in duration. To hear more about this Manufacturing Shift Supervisor job, please contact Bethan on 01438 723500 or email bherbert@ckhealthcare.com quoting reference HC19199. 139 North London, UK CK Clinical 2010-02-01T03:45:22-08:00 19267 2010-01-29T05:52:04-08:00 A US headquartered global professional services firm is trying to hire a Director of BI/DW Technology for their life sciences practice. Requires strong technology underpinnings Experience with a top tier professional services firm where you have controlled business development for a large part of a life sciences practice Recent Business Intelligence/Data Warehouse technology experience Has carried a P&L of at least $30 million There is a significant base compensation offered with this position plus bonus. Email resume in Word to TheBigGameHunter@cisny.com. Please include the job code for the position with your resume. NO RELOCATION. NO VISA TRANSFERS. NO OVERSEAS RESUMES. NO 3RD PARTIES. To receive a complimentary subscription to my job search ezine, No B.S. Job Search Advice, go to www.JeffAltman.com to subscribe. Receive tweets from Twitter with job search tips -- TheBigGameHuntr 138 Hubbed in New Jersey. Work in the Northeast Concepts in Staffing/The Big Game Hunter, Inc. 2010-01-29T05:52:04-08:00 19320 2010-01-28T12:30:28-08:00 Need to be proficient in SAS, have experience supporting clinical trials with respect to producing analysis datasets, tables, listing and figures. Should also be familiar with CDISC, SDTM, UNIX, CRT (item11). Capable of programming from Protocols and SAP’s with little guidance. Have great communications skills to partner with other programmers and statisticians. Proficient program, data and reporting validations skills and be able to work with outside vendors. 137 NJ, CT & DE Indotronix International Corporation 2010-01-28T12:30:28-08:00 19327 2010-01-28T11:47:51-08:00 A US headquartered global professional services firm is aggressively looking for an infrastructure consulting manager for a role that would be hubbed in the Northeastern USA. They want someone with infrastructure experience (obviously), who has delivered projects (lan, wan, data center optimization . . . projects like that; not call center) who some business development experience. They specifically want life sciences experience to go along with the consulting background. Travel is targeted to approximately 50% The base will go $120000 - $130000 plus bonus (all in should go to $150,000 - $160000). The cool thing about this job is that the person it reports to is going to be returning home overseas so there is a very definite path to senior management sooner, rather than later. Interested? Qualified? Please email your resume in Word to TheBigGameHunter@cisny.com Know someone for whom this is a better fit? Feel free to forward this email to them with my thanks. 136 Northeastern USA Concepts in Staffing/The Big Game Hunter, Inc. 2010-01-28T11:47:51-08:00 19320 2010-01-28T04:42:28-08:00 A rare opportunity has arisen for an experienced Project Statistician to work with one of the world’s leading Pharmaceutical companies. In this role the Project Statistician develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, veterinarians, and/or medical colleagues. The Project Statistician is responsible for working with research associates and scientists to establish a reporting database and for analysing data for these types of studies. The main responsibilities of this Project Statistician job are outlined below: Statistical Trial Design and Analysis • Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study. • Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol, and conducting the actual analysis once a reporting database is created. • Collaborate with data management in the planning and implementation of data quality assurance plans. • Maintain currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected. • Participate in peer-review work products from other statistical colleagues. Communication of Results and Inferences • Collaborate with team members to write reports and communicate results. • Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings. • Respond to regulatory queries and to interact with regulators. The ideal candidate for this Project Statistician job will be educated to an M.S or Ph.D. degree standard in a Statistics or Biostatistics discipline, or will have equivalent experience, along with proficient knowledge in the SAS programming language. Further competencies required for this role include: • Interpersonal communication skills for effective customer consultation. • Teamwork and leadership skills. • Technical growth and application with working knowledge of experimental design and statistics. • Self-management skills with a focus on results for timely and accurate completion of competing deliverables. • Resource management skills. • Creativity and innovation. • Demonstrated problem solving ability and strategic thinking. • Business process expertise associated with critical activities (e.g. regulatory submissions). If you would like to hear more about this project statistician role, please contact Sarah Brunnen at CK Clinical on 01438 743047 or email sbrunnen@ckclinical.co.uk. About CK Clinical Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. • Visit our website at: http://ckclinical.co.uk/ • Follow CK Clinical on Twitter: http://twitter.com/CKClinical • Join the Linkedin CK Clinical LinkedIn Group: http://bit.ly/FMj4z • Become a fan of CK Clinical on Facebook: http://bit.ly/1MXAE5 • To meet some of our consultants and hear more about our current vacancies, visit our YouTube: http://www.youtube.com/CKclinical Keywords: project statistician, statistician, ck clinical, pharmaceutical, pharmaceutical recruitment, pharmaceutical jobs, job, jobs, uk, Statistical Trial Design and Analysis, surrey, south east, data analysis, SAS programming language, regulatory submissions, pharma jobs. 135 South East, Surrey, UK CK Clinical 2010-01-28T04:42:28-08:00 19267