Are you a business? Hire clinical trial supply associate candidates in Montclair, NJ
Gathers, informs, and acts on clinical/medical/scientific insights for clinical trial concept ... To the clinical operations team in the country, especially to the Clinical Research Associates, and ...
Summary The Associate Director CD DEI CoE will support the Head, CD DEI CoE in defining and ... Support the visibility of Clinical Trial Diversity activities across Novartis, and ensure buy-in ...
The Associate Expert Drug Supply is responsible for production of patient derived clinical cellular immunotherapy products by functioning as both operator and verifier. Associate Expert Drug Supply ...
... Trial Directors, Safety Leaders, Biostatisticians and Regulatory Directors. In addition, you will ... If the associate is remote, all home office expenses and travel/lodging to the East Hanover or ...
Oversee/conduct medical and scientific review of trial data with Clinical Scientific Expert (CSE). May be the Program Manager of other associates (e.g.., CSE). May function as study medical monitor
Driving execution the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where ...
Drive execution of the program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors, and regional/country medical associates * Support the Global Program ...
Driving execution of the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates ...
Act as C-ISRC reviewer for relevant clinical trial concept sheet and protocol reviews. * Expected travel up to 20% Requirements: * Master's degree in a relevant field such as life sciences, business ...
... associates * Ensures ongoing medical and scientific review of clinical trial data * Supports (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section, may be a core member of ...
... associates globally. TM plays a pivotal role in bringing innovative medicines to patients, by ... Responsible for implementation of best practices and standards for trial management and clinical ...
May act as an operational and/or functional manager of associates including providing supervision ... clinical trial/program, and able to summarize and discuss status of deliverables and critical ...
