- Integrated Resources, Inc (Cambridge, MA)
- …Cambridge, MA Duration: 8+ Months Job Description: Duties: . Reporting to the Associate Director , Drug Safety and Pharmacovigilance Compliance and ... with document development requirements are identified and aligned to overall strategic objects. . Assists with monitoring DSPV compliance with regulations, PV… more
- Boehringer Ingelheim (Athens, GA)
- … 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...ensure compliance with all regulations and laws worldwide on Pharmacovigilance (including but not limited to FDA 21 CFR,… 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 ... accredited institution and more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or DO degree or international… 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
- 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
- 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 ... with FM Plans in alignment with high priority regional business needs + Provides strategic input and insights as part of compliant collaboration across the matrix in… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Program Leader (CPL) - Retinal health, assumes full medico-scientific and strategic leadership of clinical programs with the objective to accelerate clinical ... 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)
- …Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance , Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational ... Services, Project Management and Operational Management. Develop a strong, positive strategic business partnership with the global R&D business and Global IT… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global ... 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS)… more
- Amgen (Washington, DC)
- …assigned product(s) and or setting the strategy, direction, and priorities of pharmacovigilance activities. + Manage Medical Directors, Associate Med Directors, ... for a career you can be proud of. Senior Director Global Safety **Live** **What you will do** Let's...you will establish the strategy, direction, and priorities of pharmacovigilance activities and are accountable for the overall safety… more
- Sanofi Group (Cambridge, MA)
- **Clinical Research Director - allergy-immunology-dermatology** The Clinical Research Director (CRD) is noted as the **primary clinical expert for programs** . ... The role requires a well-organized, strategic and operationally focused, resourceful individual with very good...clinical study report + Take on as necessary the Associate CRD role: + Develop the abbreviated protocol +… more
- Novo Nordisk (Plainsboro, NJ)
- …shaping efforts, and pre-launch planning for pipeline assets. Relationships Reports to Associate Director / Director , Strategic Market Insights. Supports ... ready to maximize your potential with us? The Position As a member of the Strategic Market Intelligence team, the primary purpose of this role will be to become a… more
- Amgen (Washington, DC)
- …the Board of Directors. The Manager will collaborate with the Senior Manager and Director of Patient Access on PAP operations and will need strong project management ... to day oversight of program specific PSP at Amgen Inc. (eg pharmacovigilance ). + Ensure efficiency and compliance controls associated to Foundation approved policies… more
- Merck (Austin, TX)
- …safe, effective, innovative medicine. The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC ... **Job Description** Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare...+ Standards development teams and data governance reviews + Strategic and process improvement/design projects + Industry forums and… more
