- 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
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to case processing activities. Relationships Reports to the Executive Director , NAO Patient Safety with cross-functional working relationships within Medical, ... Legal and IT. This person will provide direct guidance to a team of Associate Managers, intake associate managers and directly and indirectly to case processing… more
- Merck & Co. (Rahway, NJ)
- …effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC Controlled ... Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global...and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …efforts, and pre-launch planning for pipeline assets. Relationships Reports to Associate Director / Director , Strategic Market Insights. Supports current ... Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent,… 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 ... + Form strategic alliances with key internal stakeholders as needed (eg: Pharmacovigilance , Regulatory Affairs, Global Strategic Marketing, Quality Assurance and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …you with the opportunity for significant professional development. The (Senior Associate ) Director is a key member of global , cross functional product teams ... of team members, review of team output + Represent Global Pharmacovigilance in internal and external committees...be hired_** **_at level commensurate with experience and education._** ** 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...Director in PV Sciences. At the forefront of pharmacovigilance innovation, we offer a dynamic and collaborative environment… 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 ... in areas relevant to drug discovery or development, eg epidemiology, toxicology, pharmacovigilance , regulatory affairs + Experience within Global Patient Safety… more
- Lilly (Indianapolis, IN)
- …develop creative solutions to support communities through philanthropy and volunteerism. Associate Director / Director , External Collaborations will lead ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… 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 ... safety scientist * Pharmaceutical product development experience * Experienced in global regulatory requirements for pharmacovigilance **Travel:** Less than 10%… 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 ... and execution of certain post-marketing commitments and ensuring compliance with global regulatory requirements. **Position Summary** Leads Safety Data Review (SDR)… 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 ... 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
- Amgen (Washington, DC)
- …and priorities of pharmacovigilance activities. + Manage Medical Directors, Associate Med Directors, and/or Global Safety Physicians (GSP). + Accountable ... time for a career you can be proud of. ** Global Safety Medical Senior Director , Obesity -...you will establish the strategy, direction, and priorities of pharmacovigilance activities and are accountable for the overall safety… 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 ... global CREA Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...years of applicable experience, required. + Leadership experience required. ** Director Requirements:** + US MD or DO degree or… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Associate Director , External Research, Scientific Affairs provides strong subject matter expertise, operational oversight and process ... in the process. + ER Trial Protocol + Leads and works cross functionally with Global Pharmacovigilance , CDMA TA Medical, and RA to review the trial protocol and… more
- Bristol Myers Squibb (Minneapolis, MN)
- …market with a focus on patients suffering with schizophrenia. BMS is a global biopharmaceutical company leading the way in medical innovation to help patients live ... and spirit of independence and love of challenge. **Job Description** The Region Director (RD) is a remote leadership position that is primarily responsible for… more
- AbbVie (North Chicago, IL)
- …Description In collaboration with a therapeutic area Medical Director or Scientific Director , the Associate Director or Clinical Scientist II, will lead ... the design, conduct, analysis, and reporting of clinical trials. The Associate Director , Clinical Science will apply scientific training and clinical research… 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 ... and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering… 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 ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...vendor selection decisions. + Work closely with PE Sr Director and/or delegates to identify operational gaps & drive… more
