- Takeda Pharmaceuticals (Boston, MA)
- …+ Minimum of 5 years prior experience in pharmaceutical industry in a drug safety / pharmacovigilance global setting + Experience in developing procedural ... Ensures adequate training support to all functional areas within Patient Safety & Pharmacovigilance (PSPV) in a Pharmacovigilance (PV) regulated environment.… more
- Sumitomo Pharma (Raleigh, NC)
- …English. **Education and Experience** + **Medical Degree (MD) with 3-5 years of drug safety experience in a pharmaceutical company** + Experience in oncology ... Evaluation and Mitigation Strategy (REMS) + Contributes to PVRM and cross-functional drug development teams and manages Safety Charters + Handles Health… more
- Amgen (Washington, DC)
- …Analytics Center (DAC). Observational research (OR) makes important contributions to drug development, commercialization, and safety evaluation. OR gives ... products. + Designs and implements retrospective database studies in support of safety and pharmacovigilance . + Provides epidemiological input to worldwide… more
- Ascendis Pharma (Princeton, NJ)
- …2 days remote. Key Responsibilities + Assists Head of GPS Medical Science for drug safety and pharmacovigilance activities for ensuring corporate compliance ... workplace for employees to grow and develop their skills. Associate Director, Global Patient Safety Medical Science...product safety . + Supports the development of safety surveillance and risk management plans for drug… more
- United Therapeutics (Phoenix, AZ)
- …are passionate about PV and enjoy being part of a collaborative team. The Associate Global PV Case Management Director plays a key role in management and oversight ... of end-to-end case safety management activities spanning across our global commercial product...is critical in ensuring that commercial operational aspects of pharmacovigilance activities are managed with rigorous global standards in… more
- Takeda Pharmaceuticals (Boston, MA)
- …Affairs, Regulatory Affairs, Biostats) to ensure alignment of global position for pharmacovigilance risk management processes to maximize patient safety + ... 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… more
- Rhythm Pharmaceuticals (Boston, MA)
- …with an advanced understanding of requirements for clinical trials and drug development, regulatory submissions, pharmacovigilance reporting and medical ... barriers, together. Opportunity Overview Rhythm seeks an experienced and highly motivated Associate Director of Medical Writing (MW) who can independently develop as… more
- Haleon (Warren, NJ)
- …supplements. In line with a risk-proportionate framework for product vigilance, the ** Associate Director, Consumer Safety Science** is accountable for developing ... for medium to high-risk products. The position holder will: + Develop safety strategy for medium to high-risk products within the assigned therapeutic category… more
- Amgen (Washington, DC)
- …unit setting **Or** Associate 's degree (ADN) and 10 years of Safety / Pharmacovigilance or Clinical Research experience in a hospital, university or clinical ... the execution of clinical pharmacology studies including bioequivalence, special safety , food-effect, drug - drug interaction, special...DNP) OR PharmD OR MD and 2 years of Safety / Pharmacovigilance or Clinical Research experience in a… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. The purpose of the Associate /Senior Associate /Principal Associate - MQO is to support the development ... + Understand the roles and responsibilities of the EU Qualified Person for Pharmacovigilance (EU QPPV), if applicable. + Serve as an IT systems business quality… more
- AbbVie (North Chicago, IL)
- …to support potential product related issues *Key medical quality interface with Pharmacovigilance & Patient Safety (PSEQ), Global Medical Affairs (GMA) and ... drug risk management and/or medical device/ combination product vigilance ( safety signal detection, data mining techniques, pharmacovigilance / device… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and other vendors to ensure high quality ... possesses advanced knowledge of medical terminology capture and reporting of safety data, pharmacovigilance , industry best practices, and relevant regulatory… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …of data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and other vendors to ensure high quality ... possesses advanced knowledge of medical terminology capture and reporting of safety data, pharmacovigilance , industry best practices, and relevant regulatory… more
- ThermoFisher Scientific (Wilmington, NC)
- …find cures for cancer. **Location/Division Specific Information** Our detailed, goal-oriented Pharmacovigilance colleagues manage the safety profile of new drugs ... experience working on clinical trials through every stage of drug development. This includes management and oversight of all...years) in the industry; Or + Direct experience in safety / Pharmacovigilance (comparable to 2 years) + Experience… more
- Boehringer Ingelheim (Ridgefield, CT)
- …DNP, DO, Ph.D., Master's) preferred + Specialized Pharmacist or Master of Drug Regulatory Affairs, RAC certification preferred ** Associate Director Experience ... will also provide US strategic regulatory guidance to facilitate efficient and compliant drug development and product maintenance as well as act as primary company… more
- AbbVie (South San Francisco, CA)
- …integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... and responses, and other program documents. + May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical Scientists working on the same… more
- AbbVie (North Chicago, IL)
- …integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... and responses and other program documents. + May oversee the work of Associate Medical and/or Scientific Directors and of Clinical Scientists working on the same… more