- Takeda Pharmaceuticals (Trenton, NJ)
- …innovation-driven company to inspire you and empower you to shine? Join us as an Associate Director , GCP Compliance based remotely reporting to the ... Director , GCP Compliance . At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more
- Novo Nordisk (Plainsboro, NJ)
- …to the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring ... and other key internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing relationships with internal… more
- Penn Medicine (Plainsboro, NJ)
- …study team meetings, disease site and/or discipline group meetings, and ongoing protocol training/ compliance meetings. The Associate Director will assist in ... future each day. Are you living your life's work? We are hiring for an Associate Director Oncology Research Operations to join our Cancer Services team at Penn… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... you will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department… more
- Conviva (Trenton, NJ)
- …a part of our caring community and help us put health first** The Associate Director , Security Architecture will play a key role in implementing security ... frameworks to ensure the enterprise can achieve the enterprise security strategy. The Associate Director , Security Architecture will play a key role in… more
- Bristol Myers Squibb (Princeton, NJ)
- …by leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... Director of Informed Consent Management. The AD will be...both patient safety and quality, and specimen and data compliance . + Independently liaise with Regional Country Operations to… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** ** Associate Director , Clinical Scientist** This position drives scientific planning, strategy and execution of ... interpretation of clinical data/medical protocol deviations in collaboration with the Clinical Director . + Builds talent and capabilities of direct and indirect team… more
- Merck (North Wales, PA)
- **Job Description** The Associate Director , Business Analyst, within Metrics, Analytics & Performance (MAP) will lead activities related to the development, ... + Knowledge of the Drug Discovery Process, ICH and GCP guidelines. + Strong understanding of how metrics can...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance **Los… more
- Merck (West Point, PA)
- …experience + Strong knowledge of Clinical Development through submission Process, ICH, GCP guidelines and CFR 21 regulations related to Clinical Development and ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance **Los Angeles Residents… more
- University of Pennsylvania (Philadelphia, PA)
- …(CRU)- Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will work ... and quality of research. + The candidate will work closely with the CRU Associate Director of Operations to develop and implement SOP's, report team study… more