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Responsible for aspects of clinical trial including key data management activities in compliance with GCP's, SOPs and standards within established timelines, and budgets. The CTOM is involved in the scientific..
The Manager of Print Production is responsible for managing the print process and ensure timelines are captured and met from development through the review process, production and dissemination. Exceptional communication..
The mission of Customer Service (CS) is to provide compassionate, knowledgeable and efficient service to consumers and healthcare providers to maintain and enhance the use and prescribing of Sanofi U.S...
The candidate must have excellent Chemistry, Manufacturing and Controls (CMC) technical writing and communication skills with a strong background in pharmaceutical manufacturing, regulatory writing or quality control/quality assurance with at..
Under the supervision of the Learning Head the Training Assistant (TA) supports GPE PV QTC in ensuring that the GPE fulfills it's responsibilities towards training. The TA is responsible of..
Position: Emerging and Changing Regulations Contractor Manager: Manager, Global GMP/GDP Compliance 1. PURPOSE AND SCOPE OF POSITION: This position is responsible for managing and administering the Emerging/Changing Regulation Process. 2...
Duties: Deliver quality research projects, economic models, trial design recommendations and other activities in support of programs/products. The incumbent interfaces with Clinical, Medical Affairs and business partners including Marketing, External..
Responsibilities will include, but are not limited to, the following: Assist and lead the development, management, design, implementation and delivery of health outcome strategy & tactical plans for specific product(s)..
The Clinical Data Associate Principal position requires a highly skilled individual, who seeks a technical rather than a managerial career path. Will often be responsible and play a key role..
NOTE: The manager can be flexible on how much the person can be onsite(for the right person), but preferably he would like 3x per week. Must have high level global..
Individual is expected to perform in vitro and in vivo assays to contribute towards the discovery and preclinical evaluation of immunotherapeutics and vaccines targeted against disease resulting from bacterial infection...
Creation and revision of GMP documentation including Production Batch Records, Standard Operating Procedures, and related documentation. Coordination of timelines, document revisions and review cycles for all GMP documents including delegation..
The Senior CTOM is responsible for the overall operational planning and activities for the implementation and conduct of studies (R&D clinical trials or Medical Affairs clinical trials, observational studies, compassionate..
Job Title: Clinical Trial Associate - NJ Duration: 6 months Location: Summit, NJ Job#: CELGJP00006192 Responsibilities will include, but are not limited to, the following: Prerequisites: Completed BA/BS in directly-relevant..
Job Title:u00a0Clinical Trial Associate - NJ Duration: 6 months Location: Summit, NJ Job#:u00a0CELGJP00006192 Responsibilities will include, but are not limited to, the following: Prerequisites: Completed BA/BS in directly-relevant discipline or..
The Clinical Trial Operations Manager (CTOM) is responsible for all aspects of clinical trial including key data management activities in compliance with GCP?s, SOPs and standards within established timelines and..
Actual Job Title = Data Research Associate DURATION = one year from start date Job LOCATION = Cambridge, MA Typical Daily Work Hours = 8am to 5pm (with some flexibility..