- Boehringer Ingelheim (Athens, GA)
- …+ Form strategic alliances with key internal stakeholders as needed (eg: Pharmacovigilance , Regulatory Affairs, Global Strategic Marketing, Quality Assurance and ... The AD Global PV Data Analysis supports the Global Pharmacovigilance (PV) team to ensure compliance with all regulations...and local PV Teams as needed. + Work with Quality Teams to investigate any relevant drug safety and/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...Director in PV Sciences. At the forefront of pharmacovigilance innovation, we offer a dynamic and collaborative environment… more
- BeiGene (San Mateo, CA)
- …in departmental activities **Supervisory Responsibilities:** The position has no direct reports. The Associate Director , Safety Scientist is part of a team that ... signal evaluation/safety monitoring activities and contributes and assists in pharmacovigilance activities including benefit/risk and regulatory activities and interactions._… 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 ... documents for new and expanded indications (Filing Activities). Ensures pharmacovigilance regulatory compliance. Mentors less experienced scientists and teams in… 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 ... new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific… 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 ... sources + Consult and coordinate with the Device Surveillance Senior/Executive Director and Device Safety Physician to facilitate appropriate signal management of… 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
- Lilly (Indianapolis, IN)
- …may impact a positive benefit-risk balance for a given product. The Associate Director Pharmacoepidemiology Study Operations (AD Ops)is responsible for providing ... scientists and Research and Development Operations (RD Ops) /Procurement/ Quality in the contracting of PE studies to external...vendor selection decisions. + Work closely with PE Sr Director and/or delegates to identify operational gaps & drive… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , Medical Coding, Analytics & Process is responsible for ... medical coding data, develop, and maintain metrics and algorithms to measure coding quality and support quality review. The incumbent will provide insights,… more
- 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 ... collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and External Vendors for the data services...on behalf of Daiichi Sankyo. This position also ensures quality delivery of all 3rd party data from diverse… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Established Brands Associate Director is responsible for strategy and execution of ... risk/benefit of assigned products regarding new indications, safety or stability/ quality issues, medical necessity/sensitivity assessments or other actions that… more
- Boehringer Ingelheim (Ridgefield, CT)
- …of the Evidence team. The incumbent will drive patient value, patient voice and quality of life & outcomes in line with Medicine Excellence goals. The optimal ... of cross-functional evidence team (Clinical Operations, Biostatistics, Translational Medicine, Pharmacovigilance , Regulatory, Medical Affairs, Market Access, Epidemiology, RWE etc)… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS) ... with Global Labeling Operations and Compliance Leads to produce high quality labeling documentation. + Establishes Processes and Best Practices: Reinforces labeling… 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
- AbbVie (North Chicago, IL)
- …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 ... key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality… more
- AbbVie (Mettawa, IL)
- …and responses and other program documents. + May oversee the work of Associate or Assistant Scientific Directors and of Clinical Scientists working on the same ... key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality… more
- University of Maryland, Baltimore (Baltimore, MD)
- …of Pharmaceutical Sciences with teaching responsibility to the Graduate Program Director and Associate Dean for Graduate Programs. *_ACADEMIC RESPONSBILITIES ... science, including: Chemistry, Manufacturing, and Controls (CMC); Clinical Research; Pharmacovigilance ; Phase IV Research (eg, Pharmacoepidemiology); and Drug and… more