- Amgen (Washington, DC)
- …patients worldwide. It's time for a career you can be proud of. **Global Pharmacovigilance (PV) Senior Scientist , Obesity - US Remote** **Live** **What you will ... world. In this vital role the Global PV Senior Scientist will work within the Therapeutic Safety Teams and...**Basic Qualifications:** Doctorate degree and 2 years of safety/ pharmacovigilance experience OR Master's degree and 4 years of… more
- Astellas Pharma (Northbrook, IL)
- …data from ongoing clinical studies at each SMT + Working with the Pharmacovigilance Scientist , PV Risk Management and Pharmaco-Epidemiology, the EDSP oversees ... of Proof of Concept. As the compound lead within Pharmacovigilance , the EDSP serves as the primary liaison for...as the primary liaison for other members of the Pharmacovigilance team, to ensure the communication of key compound… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Clinical Scientist **Location:** Cambridge, MA **About the Job** Are you ready to shape the future of medicine? The race is on to speed up drug ... Development Units in Sanofi R&D. The primary purpose of the Clinical Scientist 's position is to assist/support the Clinical Research Director in the… more
- BeiGene (San Mateo, 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
- Amgen (Washington, DC)
- …Join us and transform the lives of patients while transforming your career. **Senior Data Scientist ** **What you will do** We are seeking a Senior Data Scientist ... modeling, or causal modeling may receive special consideration. Domain knowledge in Pharmacovigilance or at least one of biopharmaceutical R&D discipline is strongly… more
- Actalent (Rockville, MD)
- …Clinical Operations, Statistical and Scientific Innovation, Regulatory Affairs, and Pharmacovigilance . + Author abstracts and manuscripts for publication in ... peer-reviewed journals and/or presentation at scientific association meetings. + Review and synthesize complex information from scientific literature in support of protocol development and use scientific expertise to prepare, present, and define complex… more
- Merck (Rahway, NJ)
- …(eg, Medical Affairs, Regulatory Affairs, Clinical, Pharmacovigilance ). Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld) Current ... Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld) **US and Puerto Rico Residents Only:** Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.… more
- AbbVie (South San Francisco, CA)
- …or related programs. + Ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards ... in conducting research. Contributes to authorship of regulatory responses and actively participates in meetings. + Oversees project-related education of investigators, study site personnel, CRO partners and AbbVie study staff. + Has responsibility for review,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and accountable for the definition and execution of the worldwide pharmacovigilance strategy for all Gilead investigational and marketed products. The GHPS ... area trends and their relevance to the Gilead portfolio; Provides pharmacovigilance leadership, oversight, strategic and technical guidance in discussions with teams… more
- Bristol Myers Squibb (Princeton, NJ)
- …for ensuring the safety of our medicines. This includes all pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety ... Partners with WWPS personnel at similar leadership level (Case Management Leads, PV Scientist Leads, and SMT Chairs, MSA TA Heads) and personnel from other functions… more
- Bristol Myers Squibb (Princeton, NJ)
- …for ensuring the safety of our medicines. This includes all pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety ... OpEx, Head of PVOpS Data Acquisition and Interfaces, PV Scientist Leads, and SMT Chairs, MSA TA Heads) and...product safety with a track record of working in pharmacovigilance + Knowledgeable of ICH Guidelines and relevant US… more
- Pfizer (Collegeville, PA)
- …director works closely with other functions such as regulatory affairs, pharmacovigilance , biostatistics, and medical affairs to ensure that the clinical development ... RESPONSIBILITIES:** Study-level Clinical Development Leadership + Collaborate with Clinical Scientist (s) to provide clinical leadership across 2-3 study team(s) that… more
- Gilead Sciences, Inc. (Foster City, CA)
- …: You will learn about core Patient Safety Oncology pharmacovigilance activities, including signal detection, benefit-risk evaluation, risk management plans ... under the close supervision of an experienced Global Therapeutic Area (TA) Safety Scientist or Physician. **Key Responsibilities will include, but are not limited to… 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
- BeiGene (Emeryville, CA)
- …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
- BeiGene (Emeryville, 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
- Gilead Sciences, Inc. (Foster City, CA)
- …some of these responsibilities with supervision from a more experienced Safety Scientist or Physician. You will help ensure that safety documentation is stored ... safety signal detection and management, Good Clinical Practices (GCP) and Good Pharmacovigilance (GVP). + Knowledge of MedDRA applications / uses. + Demonstrates… 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
- BeiGene (Emeryville, 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
- BeiGene (Emeryville, 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
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