A Statistical Programmer with SAS programming skills is needed for a 6-month contract position at major pharma company in Northeast.
The Statistical Programmer is responsible for providing significant programming support to the statisticians as part of the contribution towards the completion of statistical analyses (tables, listings and figures) and reporting of results of clinical studies. It includes Safety, Immunogenecity and Efficacy Analysis. In addition, other ad hoc analysis may have to be ...
Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. And driven to make a difference, from innovative research to ...
Description The Regulatory Affairs Associate works effectively under Regulatory Strategic Development (RSD)
Work independently (under the limited supervision of a Regulatory Manager or above) to:
Organize documents and records to be included in regulatory submissions.
Provide upkeep of regulatory archives Assist in the preparation of paper and electronic submissions for regulatory authorities
Track due dates of routine submissions.
Prepare and submit routine regulatory documents to FDA, e.g. ...
Our client in Titusville, New Jersey is looking for a Project Physician.This is a long term consulting position.If interested, Please apply to this ad
Position: Project Physician
Location: Titusville, New Jersey
The Project Physician is a responsible member of a clinical team (Compound Development Team, CDT)) and reports to the CDT Leader. The PP will be dedicated to working with the team to manage the execution of a Phase 3 Efficacy and Safety Study of an anti ...
Jun 5 -
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