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Responsibilities: Implement and execute methodological and statistical aspects of clinical studies with direction from Therapeutic Area Head / Deputy (TAH / TAD) or project lead statistician. Provide leadership and guidance on statistical matters to interdepartmental clinical / regulatory teams. In some cases princ ... Job Role: Maths & IT | Job Hours: Full-Time | Sector: Industry | Location: PA - Pennsylvania | Published Date: Monday, December 03, 2007 1:49:10 PM
Responsibilities: This position is responsible in the US for the business development for sanofi-aventis API (Active Pharmaceutical Ingredient) sites. This position has responsibility for identifying, planning, and securing large pharmaceutical manufacturing accounts, as well as working with a team of cross-functio ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 2:09:18 PM
Responsibilities: JOB SUMMARY - Working semi-independently in the RA Pain Pharmacology section in Internal Medicine, carry-out/oversee in vivo pharmacological studies (compound enabling/validation/provision of materials) for programme advancement in the area of inflammatory and neuropathic pain. - Plan studies and ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Wednesday, July 25, 2007 11:00:00 PM
Responsibilities: JOB SUMMARY The primary function of the Risk Management Plan Officer's (RMPO) role is to define the product risk management strategy, to champion this strategy within the Company, to elaborate, maintain and update the risk management plans (or waivers thereof) to be submitted to the competent Auth ... Job Role: Other | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 11:42:00 AM
Responsibilities: Sanofi-aventis has an opportunity in the new Commercial of, Industrial Affairs organization. The Director of External Pharmaceutical Production, as a virtual plant manager is responsible for the production of finished product made at third parties for sanofi-aventis. This position is responsible f ... Job Role: Engineering | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 1:57:19 PM
Responsibilities: Serve as liaison and direct contact between the company and the FDA for oncology products. Provide regulatory leadership to project teams to ensure the logical development and clear delivery of a unified position for regulatory strategy, submissions, and Agency interactions. Lead project team to c ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: PA - Pennsylvania | Published Date: Monday, December 03, 2007 2:02:04 PM
Responsibilities: Responsible for successful implementation and operational aspects of Phase I to III clinical studies in the United States. Direct/lead the Team to ensure successful completion of US Phase I, II and III clinical trials in a timely, ethical, and a scientifically responsible fashion. Evaluate feasib ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: PA - Pennsylvania | Published Date: Monday, December 03, 2007 2:07:35 PM
Responsibilities: Position Summary: The Manager of International Trade Compliance is responsible for managing significant activities within the sanofi-aventis International Trade Compliance group in order to develop and maintain a robust Trade Compliance Program, including: (i) prevention, detection, and correction ... Job Role: Other | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 1:02:51 PM
Responsibilities: Job Summary: This position is responsible for supporting the local Clinical Packaging Operations (CPO) group production of finished packaged investigational product ready for shipment to worldwide study sites, CRUs and CROs. The position interfaces, on a constant basis, primarily with Supply Chain ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: PA - Pennsylvania | Published Date: Monday, December 03, 2007 2:06:05 PM
Responsibilities - Working under the direction of AVP, supervise the conduct of clinical trials. Support marketing, sales, regulatory, and legal functions through provision of medical expertise concerning marketed products and drugs that are in approval process. - Assists and coordinates the utilization of scientif ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 1:32:29 PM
Responsibilities: JOB SUMMARY The SMA Clinical Q&C Senior Specialist is responsible for the initiation, conduct, and follow-up of audits as assigned by C Q&C Management, including all interaction with involved operational staff (e.g. Project Teams, Clinical Operations, Pharmacovigilance, etc.) within the frame of t ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 1:50:36 PM
Responsibilities: Job Summary: Provide support in a team environment to the Logistics Group within Sanofi-Aventis Research, primarily in the area of planning. Incumbent will be the GMPK-US/KW Department Logistics (DL) for Bridgewater, Great Valley, and Kawagoe and will be expected to manage the departmental OPX2 da ... Job Role: Other | Job Hours: Full-Time | Sector: Industry | Location: PA - Pennsylvania | Published Date: Monday, December 03, 2007 11:54:52 AM
Responsibilities: JOB SUMMARY Responsible for the operation of the chromatography lab including: Chiral and achiral chromatography method development both preparative and analytical, chiral purification by LC and SFC. Also responsible for scheduling work and setting priorities as well as overseeing the work of the ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 11:53:42 AM
Responsibilities: JOB SUMMARY Under lab head supervision, carry out compound enabling experiments on GPCRs including cAMP, radioligand binding, FLPR and GTPgammaS studies. Outline & plan studies, execute experiments in timely fashion, analyze & provide high quality data to supervisor & programme team. With supervis ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 1:33:36 PM
Responsibilities: JOB SUMMARY Under the supervision of the Quality Control Manager in PRCU, the Quality Control Officer participate in the definition and implementation of a quality control system in GPE to maintain the highest possible quality of GPE outputs. In particular the QC Officer dedicated to Case manageme ... Job Role: Biology | Job Hours: Full-Time | Sector: Industry | Location: NJ - New Jersey | Published Date: Monday, December 03, 2007 12:59:33 PM
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