- Takeda Pharmaceuticals (Boston, MA)
- …life-changing therapies to patients worldwide. Join Takeda as a **Senior** **Principal Pharmacovigilance Scientist ** where you will provide pharmacovigilance ... will contribute:** + Technically fully competent to perform all usual Principal Pharmacovigilance Scientist /Senior Pharmacovigilance Scientist workload,… more
- Sumitomo Pharma (Lincoln, NE)
- …. **Job Overview** The Senior Manager, Pharmacovigilance Scientist serves as the ... and at partner meetings including Joint Safety Forums (JSFs) and Pharmacovigilance Committee (PVC) meetings. + Review adverse event reports-including serious… more
- Amgen (Washington, DC)
- …Join us and transform the lives of patients while transforming your career. Global Pharmacovigilance (PV) Scientist **What you will do** Let's do this. Let's ... applications and other regulatory filings + Assist GSO/ or other Senior Scientist in developing a strategy for safety-related regulatory activities + Provide safety… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. **Global Pharmacovigilance (PV) Senior Scientist ** **What you will do** Let's do this. ... these qualifications. **Basic Qualifications:** Doctorate degree and 2 years of pharmacovigilance experience Or Master's degree and 6 years of pharmacovigilance… more
- BeOne Medicines (San Mateo, CA)
- …biological science and 4+ years of experience as a Safety ( Pharmacovigilance ) Scientist .ORMD (or internationally recognized equivalent) plus accredited residency ... **General Description:** _The Associate Director, Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages clinical… more
- Lilly (Indianapolis, IN)
- …people around the world. The purpose of the Sr. Director - Safety Data Scientist role is to provide strategic leadership for the technology, systems, automation, and ... functional areas in GPS. The Sr. Director Safety Data Scientist provides strategy, oversight, and expertise for the GPS...elevate the profile of GPS and the science of pharmacovigilance as an essential obligation of the company by… more
- Amgen (Washington, DC)
- …and transform the lives of patients while transforming your career. **Global Safety Senior Scientist ** **What you will do** Let's do this. Let's change the world. In ... this vital role the Global PV Sr. Scientist works with the Therapeutic Safety Teams for safety...of role and responsibility + Processes and regulations for pharmacovigilance and risk management + Drug development and lifecycle… more
- BeOne Medicines (Emeryville, CA)
- General Description: _The Director, Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages clinical and ... integrated Benefit/Risk assessments. + Promote and Advance the Field of Pharmacovigilance . + Responsible for effective execution, communication and influence with… 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
- United Therapeutics (Des Moines, IA)
- …an option. **Who you are** We are seeking an experienced Senior Product Safety Scientist to join our dynamic pharmacovigilance team. You will play a key ... critical thinking, medical writing, and communication skills. The Senior Product Safety Scientist will serve as a recognized leader and subject matter expert within… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** Senior Clinical Data Scientist at Boehringer Ingelheim Pharmaceuticals, Inc. in Ridgefield, CT (Telecommuting permitted: work may be performed in any ... level, including colleagues from Global Clinical Operations (GCO), Global Pharmacovigilance (GPV), TAs, Translational Medicine and Clinical Pharmacology (TMCP), and… 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
- Lilly (Indianapolis, IN)
- …and in support of the European Union Qualified Person for Pharmacovigilance (EU QPPV). **Benefit-Risk Management** **Leadership** **1) End-to-End Business Process ... internal expert to provide specialized knowledge within the area of Pharmacovigilance risk management and risk minimization activities. + Collaborate with… more
- Boehringer Ingelheim (Athens, GA)
- …(AE) reporting and request primary and follow-up information. + Provides information to pharmacovigilance and RA according to the study protocol and SOPs. + Ensures ... Regulatory Affairs to align on document organization. + Collaborates with the Scientist and study team in protocol development, CRF design, writing amendments,… more
- BeOne Medicines (San Mateo, CA)
- …clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance , regulatory, molecular diagnostics, and translational research. ... at least one study through from start to finish in a clinical scientist role + Clinical oncology experience; candidates with exceptional experience in other… 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
- Takeda Pharmaceuticals (Boston, MA)
- …may lead the US/EU Development Team but more likely will oversee the clinical scientist (s) responsible for leading this team. Emphasis will be on insuring that the ... overall safety information for studies and compounds in conjunction with Pharmacovigilance . + **External Interactions** + Directs activities involved in interactions… more
- Capgemini (Boston, MA)
- …experience while engaging with professionals in clinical research, regulatory affairs, pharmacovigilance , quality assurance, and related areas. + Build and maintain ... journey towards Intelligent Industry. Capgemini Engineering has 65,000 engineer and scientist team members in over 30 countries across sectors including Aeronautics,… more
- Takeda Pharmaceuticals (Boston, MA)
- …Development Team but more likely will oversee the study physician and/or clinical scientist leads responsible for leading the team. Emphasis will be on insuring that ... compounds. + Reviews and assesses overall safety information in conjunction with Pharmacovigilance and Medical Monitor of record for assigned compounds. + Oversees… more
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