- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **About the role:** Join Takeda as an Executive Medical Director , Pharmacovigilance in Gastrointestinal and Inflammation (GI2). You will ... and Governance. As part of the Patient Safety and Pharmacovigilance (PSPV) team, you will report to the Vice...data from internal and external studies/sources and communicates at senior leadership level the impact of same both in… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …needs and improve life by advancing the care of patients with life-threatening diseases. ** Senior Director , GVP** **Audits** The Senior Director of ... vision and strategy of the Governance, Risk and Analytics (GR&A) Team. The Senior Director 's responsibility includes leading a team of auditors, delivering an… more
- Gilead Sciences, Inc. (Foster City, CA)
- …in Patient Safety cross-functional teams. + Communicates to highest levels of senior management key pharmacovigilance findings. + Oversees or performs medical ... certification is preferred. + A minimum of 6 years' experience in pharmacovigilance with substantial knowledge of drug safety including medical review of ICSRs.… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Senior Director Clinical Development - Respiratory Date: Jan 21, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job ... a difference with. **The opportunity** This is a new Senior Director role to support the growth...closely with other functional areas such as commercial, regulatory, pharmacovigilance , CMC, early clinical and pre-clinical development in this… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The ( Senior Associate) Director will join our motivated and expert team of physicians in the global Cardio-metabolism/Respiratory Therapeutic ... you with the opportunity for significant professional development. The ( Senior Associate) Director is a key member...provide updates of the assigned drug's safety profile to senior management and recommend pharmacovigilance / risk… more
- AbbVie (Jersey City, NJ)
- …as well as PMOS. PST lead will be interpreting regulations related to pharmacovigilance supporting all patient safety activities, and will be leading the safety ... products + Lead and set the strategy for key pharmacovigilance documents, including but not limited to, medical safety...DO, not required + 5 - 8 years of Pharmacovigilance (PST lead role equivalent) / Clinical Development experience… more
- Boehringer Ingelheim (Ridgefield, CT)
- …of team output. + Provide updates of the assigned drug's safety profile to senior management and recommend pharmacovigilance / risk management activities to BI ... **Description** The ( Senior ) Patient Safety Physician will join our motivated...the global Oncology Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as a Senior Medical Director , Oncology Clinical Science in our Cambridge office. At Takeda, we ... you will be a vital contributor to our inspiring, bold mission. **OBJECTIVES:** The Senior Medical Director leads and drives strategy for the overall global… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** ** Senior Medical Director , Clinical Sciences** **Cambridge, MA** **Hybrid** **_OBJECTIVES/PURPOSE_** ... and plasma-oriented therapies for patients with serious, complex diseases. The Senior Medical Director - Hematology, Neuroimmunology & Specialty Care… 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 ... in medicine and pharmaceutical product safety with a track record of working in pharmacovigilance + Knowledgeable of ICH Guidelines and relevant US and EU PV and GCP… more
- BeiGene (Emeryville, CA)
- The Senior Director , Clinical I/O Development will support BeiGene Clinical and Medical assets by successful execution of clinical development programs and ... colleagues in clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance , regulatory, molecular diagnostics, and translational research. **Key roles… more
- BeiGene (Emeryville, CA)
- **General Description:** The Senior Medical Director , Hematology will support BeiGene Clinical and Medical Hematology assets by successful execution of clinical ... in clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance , regulatory, molecular diagnostics, and translational research. **Essential Functions… more
- BeiGene (San Mateo, CA)
- **_General Description:_** _The Senior Director , US DTC Marketing is responsible for leading the development and implementation of the patient strategy and ... to deliver highest impact + Collaborate with Regulatory, Legal/Privacy and Pharmacovigilance teams to ensure that patient initiatives comply with internal and… more
- BeiGene (Emeryville, CA)
- The Senior Director , Clinical Development, Solid Tumors will support BeiGene Clinical and Medical assets by successful execution of clinical development programs ... colleagues in clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance , regulatory, molecular diagnostics, and translational research. **Essential Functions… more
- AbbVie (Jersey City, NJ)
- …Job Description Purpose: Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading Product Safety Teams (PST) and PST leads ... signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Experts on hematology-oncology… more
- AbbVie (North Chicago, IL)
- …key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality ... standards in conducting research. Qualifications + MD or equivalent (DO) and completion of an Oncology Residency, Board certification (or equivalent in ex-US countries) preferred + 5-7 years of experience in medical monitoring of clinical trials is required or… more
- AbbVie (North Chicago, IL)
- …key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality ... standards in conducting research. Qualifications + Medical Doctor (MD), Doctor of Osteopathy (DO), or non-US equivalent of MD degree with relevant therapeutic specialty in an academic or hospital environment. Completion of a residency program strongly… more
- J&J Family of Companies (Raritan, NJ)
- …the Pharmaceuticals Chief Medical Officer (CMO), the Qualified Person for Pharmacovigilance (QPPV) Pharma, Senior Management, Health Authorities (HA), ... Johnson & Johnson, is recruiting for a Director , Medical Safety Officer, Oncology (Solid Tumor) to...or equivalent) with a minimum of 2 years of pharmacovigilance experience or other relevant experience (eg Clinical research,… more
- Novo Nordisk (Plainsboro, NJ)
- …of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring external-facing ... internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing relationships with internal stakeholders and… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Clinical Research Director **Location** : Cambridge, MA **About the Job** Are you ready to shape the future of medicine? The race is on to speed up ... could be critical in helping our teams accelerate progress. The Clinical Research Director (CRD) is noted as the **primary clinical expert for programs** . The… more