- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the ... Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and External Vendors for the data services they provide to… more
- Merck & Co. (Rahway, NJ)
- …produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC ... Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare...that the nature of the role presents an increased risk of disease transmission.Current Employees apply HERE Current Contingent… more
- Boehringer Ingelheim (Athens, GA)
- **Description** The AD Global PV Data Analysis supports the Global Pharmacovigilance (PV) team to ensure compliance with all regulations and laws worldwide on ... Pharmacovigilance (including but not limited to FDA 21 CFR,...maintaining ongoing safety surveillance program to continuous monitor the Risk /Benefit balance of our veterinary products. + Supporting Global… more
- AbbVie (North Chicago, IL)
- …Instagram, YouTube and LinkedIn. Job Description Purpose: Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading Product ... signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Responsibilities: + Understanding… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... + Clinical Overview Statements + Chair the Asset Benefit Risk Team consisting of experts in Pharmacovigilance ,...more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Sciences Pleasanton, CA, USA * Princeton, NJ, USA Req #361 Monday, April 22, 2024 Looking for a chance to make a meaningful difference in ... on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the...with the Medical Surveillance team. + Lead development/maintenance of Risk Management Plans (RMP) and associated pharmacovigilance … more
- BeiGene (San Mateo, CA)
- …departmental activities. **Supervisory** **Responsibilities:** The position has no direct reports. The Associate Director , Safety Scientist is part of a team ... signal evaluation/safety monitoring activities and contributes and assists in pharmacovigilance activities including benefit/ risk and regulatory activities and… more
- Bristol Myers Squibb (Princeton, NJ)
- …medicines: The Worldwide Patient Safety group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety ... monitoring, safety reporting, contribution to benefit- risk assessment, risk management planning and strategy, and execution of certain post-marketing commitments… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... the global Inflammation Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or… more
- Lilly (Indianapolis, IN)
- …and volunteerism. **Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage clinical and scientific expertise ... safety reviews, support for regulatory inquiries, input into device development and risk management activities, and the promotion and advancement of Global Patient… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** **Sr. Associate Director Requirements:** + US MD or DO degree or ... team of physicians in the global CREA Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of our patients worldwide. This… more
- Bristol Myers Squibb (Chicago, IL)
- …and spirit of independence and love of challenge. **Job Description** The Region Director (RD) is a remote leadership position that is primarily responsible for ... satisfaction and productivity. This position reports into a national Field Medical Director role. The RD position is underpinned with the expectation of leadership… more
- Merck (Columbus, OH)
- **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... to implement `quality by design` within clinical development programs, using a risk -based approach. The incumbent will be responsible for the overall strategy for… more
- Lilly (Indianapolis, IN)
- …impact a positive benefit- risk balance for a given product. The Associate Director Pharmacoepidemiology Study Operations (AD Ops)is responsible for providing ... of Lilly marketed products and for compounds in development. Risk management is a continuous process of assessing a...vendor selection decisions. + Work closely with PE Sr Director and/or delegates to identify operational gaps & drive… more
- Bristol Myers Squibb (Los Angeles, CA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Regional Associate Director (RAD) role is field-based and focused on ... Adverse Events (AEs) and fully understand and comply with BMS Pharmacovigilance SOPs regarding identification and reporting timelines + Contributes to managing… more
- ThermoFisher Scientific (Wilmington, NC)
- …aggregate reports, contributes to label updates, supports dossier maintenance and risk management activities. + Medically reviews adverse event and serious adverse ... to 1-2 years) in the industry. + Direct experience in safety/ Pharmacovigilance (comparable to 2 years). + Candidates with industry experience(CRO/Pharma) maybe… more
- Boehringer Ingelheim (Ridgefield, CT)
- …approvals and reimbursable medicines. Senior CPL provides continuous medical benefit and risk oversight for assigned retinal assets. In this role, Senior CPL may ... of cross-functional evidence team (Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance , Regulatory, Medical Affairs, Market Access, Epidemiology, RWE etc)… more
- ThermoFisher Scientific (Wilmington, NC)
- …aggregate reports, contributes to label updates, supports dossier maintenance and risk management activities. + Medically reviews adverse event and serious adverse ... (comparable to 1-2 years) in the industry; Or + Direct experience in safety/ Pharmacovigilance (comparable to 2 years). _Additional experience required for Sr Med … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance , Regulatory/ Risk Management, Quality Assurance, Medical Affairs, ... Translational Research, Research, Informatics Services, Project Management and Operational Management. Develop a strong, positive strategic business partnership with the global R&D business and Global IT functions of Daiichi Sankyo. As a trusted partner,… more
- Amgen (Washington, DC)
- …assigned product(s) and or setting the strategy, direction, and priorities of pharmacovigilance activities. + Manage Medical Directors, Associate Med Directors, ... you can be proud of. **Global Safety Medical Senior Director , Obesity - US Remote** **Live** **What you will...you will establish the strategy, direction, and priorities of pharmacovigilance activities and are accountable for the overall safety… more
