- Sumitomo Pharma (Nashville, TN)
- …a dynamic, highly motivated, and experienced individual for the position of Pharmacovigilance Scientist to perform PV activities for assigned programs(s). ... ongoing clinical trials. + Serve as a subject matter expert in Pharmacovigilance , including operations and medical, within the assigned program. + Support… more
- Takeda Pharmaceuticals (Boston, MA)
- …and empower you to shine? Join us as a PV Risk Management Scientist /Associate Director. At Takeda, we are transforming the pharmaceutical industry through our ... we do. As an Associate Director/ PV Risk Management Scientist , being part of our Risk Management and Benefit...Affairs, Biostats) to ensure alignment of global position for pharmacovigilance risk management processes to maximize patient safety +… more
- ManpowerGroup (Clark, NJ)
- ** Scientist ** **Clark NJ - Onsite role** **15 months contract with high potential for extension and can convert to permanent.** **Pay range: $28 - $29/hr on W2** Our ... looking for hardworking, motivated talent to join their innovative team. Are you a Scientist with a passion for collaborating with multiple teams and an interest in… more
- Lilly (Indianapolis, IN)
- …people around the world. The purpose of the Associate Director - Safety Data Scientist is to manage and analyze complex Global Patient Safety (GPS) datasets across ... trends, assess business issues, and drive analytic solutions. The Safety Data Scientist Associate Director / Director will work with stakeholders to analyze… more
- Merck (Lower Gwynedd, PA)
- **Job Description** **Job Description** Data Systems Senior Scientist (P3), Regulated Bioanalytics, Integrated Logistics & Sample Management (ILSM) **Description** ... The PDMB Regulated Bioanalytics Department is seeking a Data Systems Senior Scientist to join our Integrated Logistics and Sample Management group. This role will… more
- CVS Health (Blue Bell, PA)
- …and Aetna's Enterprise Data Warehouse (EDW). The Lead Decision Scientist role will have end-to-end responsibility of extraction-transformation-load including ... results, identify quality issues, investigate root cause, and assist Senior Decision Scientist , Senior Analyst, or Analyst in completing investigations as well as… more
- Lilly (Indianapolis, IN)
- …+ Understand the roles and responsibilities of the EU Qualified Person for Pharmacovigilance (EU QPPV), if applicable. + Serve as an IT systems business quality ... + 2+ years experience in a quality control/quality assurance role supporting Pharmacovigilance (PV) + Experience in defined functional business areas, for example,… more
- AbbVie (Chicago, IL)
- …Advisory and other similar meetings with supervision. + Proficient in pharmacovigilance regulations, guidelines, and company standard operating procedures + In depth ... understanding of compounds within assigned therapeutic areas, including safety profile and where applicable, labeling, literature, clinical and regulatory issues. This role can be remote in the US. Qualifications Qualifications: + Degree in a Health Sciences… more
- Boehringer Ingelheim (Ridgefield, CT)
- …& Clinical Pharmacology, CMC, Regulatory Affairs, Patient Safety and Pharmacovigilance to implement discovery and development toxicology strategies that enable ... the progression of optimized drug candidates. + When appropriate, take lead to develop plan and lead sub-team for investigative studies to support investigations on mechanisms of toxicity. + Serve as NDS Therapeutic Area lead, and/or provide guidance and… more
- Taiho Oncology (Pleasanton, CA)
- …the development program. + Perform data review supported by Clinical Research Scientist (s) (CRS), participate in protocol deviation meeting that will occur monthly ... cross-functional areas (eg, clinical operations, biostatistics, data management, biomarker, pharmacovigilance , quality, etc.) + Knowledge in authoring key clinical… more
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