- Merck & Co. (North Wales, PA)
- …of the QMS processes managed under GRACS(Global Regulatory Affairs & Clinical Safety) Quality &Compliance.Establishes and maintains an engaged Community of Practice ... regulations (eg, Good Regulatory Practice, Good Pharmacovigilance Practice, Good Clinical Practice,), safety guidelines and company policies and procedures.-May… more
- Tenethealth (Modesto, CA)
- …drug, dental, vision, behavioral health and telemedicine services Wellbeing support, including employee assistance program (EAP) Time away from work ... counseling Education support through tuition assistance , student loan assistance , certification support, and online educational program Additional benefits… more
- Merck & Co. (Rahway, NJ)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (Rahway, NJ)
- …management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials.- The knowledge must be ... principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions.This position involves… more
- Merck & Co. (Cincinnati, OH)
- …RMSD Team Leader - within US Medical Affairs, Global Clinical Development, Research and Development (R&D).--Primary Activities:Identify, establish and manage ... collaborative professional relationships with national, regional and clinical practice scientific leaders (SLs) and investigators to identify and address scientific… more
- Merck & Co. (Boston, MA)
- …the application of cellular, molecular technologies and models to drive program decisions.Detailed understanding of translational and clinical research ... programs, driving the Precision Medicine objectives in alignment with clinical development plans. Collaborating with Discovery, Translational Medicine and Product… more
- Merck & Co. (Sacramento, CA)
- …expertise.This position will support our Company's Gastrointestinal (GI) Immunology program .Location: The position covers the following exemplar states: WA, OR, ... policiesMaintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI)...this role at the time of this posting. An employee 's position within the salary range will be based… more
- Merck & Co. (Boston, MA)
- …strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development. The successful candidate will have an essential strategic ... strategies and interact with various stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role… more
- Merck & Co. (North Wales, PA)
- …This position supports statistical programming activities for late-stage drug/vaccine clinical development projects. This may include leadership of one or ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects.Develop and execute statistical analysis and reporting ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing… more
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