- Bristol Myers Squibb (Madison, NJ)
- …+ May serve as CTP as necessary + Accountable in partnership with the Clinical Scientist for the design, execution, and analyses of each study led by the CTPs and ... Partners with Worldwide Patient Safety physicians in the ongoing review of safety data + Serves as the (co-)leader of the cross-functional Clinical Development Team… more
- Parexel (Trenton, NJ)
- …of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client's guidelines and procedures, and global drug safety ... Indicators (KPIs) for the process + Function as pharmacovigilance representative/safety scientist + Attend/support Bid defense meetings + Actively mentoring Patient… more
- Parexel (Trenton, NJ)
- …When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist ) + May act as a Mentor for Clinical Research ... safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company's image with its… more
- Sanofi Group (Morristown, NJ)
- …in achieving corporate goals. The GPH establishes the goals and will support staff within the program and participates in strategic planning for, and oversight of, ... as interaction with regulatory/health authorities (HA), approval of documents and product label, as appropriate. In addition, the GPH will be responsible… more
- Bristol Myers Squibb (Madison, NJ)
- …landscape * The CTP should be able to anticipate impact of external data which may shift internal clinical strategy and proactively assess needs for internal ... Study-Leader with ability to own/drive study level strategic decisions * Leads medical data review of trial data , including eligibility review * Holds… more