- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... around rare diseases and immune disorders. **Summary** This position works with the Director , Clinical Study Startup to establish the strategy driving global … more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …mission? We are seeking a highly motivated individual to join us as an Associate Director , Patient Safety Risk Management. Under the guidance of the Executive ... Director of Kite Safety & Pharmacovigilance (PV),...follow-up clinical trials (LTFU), post-authorization safety studies (PASS), and global patient registries according to the evolving regulatory requirements,… more
- Ascendis Pharma (Palo Alto, CA)
- …mark. We offer a dynamic workplace for employees to grow and develop their skills. Associate Director , Medical Safety Science reports to Head of Global ... Head of Global Medical Safety Science for drug safety and pharmacovigilance activities for ensuring corporate compliance with all applicable laws and regulations… more
- United Therapeutics (Columbus, OH)
- …for cardiovascular and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Associate Global PV Case Management Director plays a key ... This role is critical in ensuring that commercial operational aspects of pharmacovigilance activities are managed with rigorous global standards in proper… 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
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... feasibility and delivery. The role supports all phases of systems development for global informatics systems, ETL and integrations. The Tech Lead must develop and… more
- Merck (West Point, PA)
- …will be responsible for managing the development and implementation of pharmacovigilance strategies, processes, and systems for a pharmaceutical company, ensuring ... PV strategies: Work with cross-functional teams to develop and implement pharmacovigilance strategies that meet regulatory requirements and ensure patient safety,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... systems, configuration and associated validation activities of Daiichi Sankyo Pharmacovigilance Safety systems, and fulfillment of data change requests.… more
- Lilly (Indianapolis, IN)
- …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 ... de-risked opportunities to evolve how Lilly and LRL operates. The **Senior Director /Executive Director ** is responsible for managing all Regulatory activities… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **OBJECTIVES:** + Ensures Global and R&D Quality processes are embedded and effectively implemented across CPMQ ... of internal functional processes and training and ensure alignment with global processes and regulatory requirements and expectations. + Drive the implementation… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …that will inspire you and empower you to shine? Join us as an Associate Medical Director Neurodegenerative Disorders in our Neuroscience Therapeutic Area Unit in ... a vital contributor to our inspiring, bold mission. **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for clinical studies… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …that will inspire you and empower you to shine? Join us as an Associate Medical Director , Clinical Science in our Gastrointestinal & Inflammation Therapeutic ... be a vital contributor to our inspiring, bold mission **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall … more
- Takeda Pharmaceuticals (Boston, MA)
- …to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Quantitative Clinical Pharmacology Lead in Cambridge, MA, where ... statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance , digital strategy, library sciences and data architecture/governance) bring… more
- ThermoFisher Scientific (Greenville, NC)
- …communities depend on - now and in the future. **Discover Impactful Work:** The ( Associate ) Medical Director will provide medical support and medical advice for ... meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission...clinical trials and safety evaluation within the Pharmacovigilance department. **A day in the Life:** + Provide… more
- AbbVie (North Chicago, IL)
- …core R&D sub-functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance , Medical Affairs, Regulatory Affairs, and Clinical Development (both ... in neurology, psychiatry, or related. Participants will enter the program as Associate Medical Directors with the opportunity to graduate into a Medical … more
- AbbVie (Chicago, IL)
- …, YouTube and LinkedIn. Job Description The Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety ... to enhance real-world methodologies and capabilities. 5. Collaborate with global epidemiology teams and key partners, including Pharmaceutical Development, Medical… more
- AbbVie (North Chicago, IL)
- …to our talent pipeline and considered for future opportunities. The Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety leads the ... to enhance real-world methodologies and capabilities. + Collaborate with global epidemiology teams and key partners, including Pharmaceutical Development, Medical… more
- Boehringer Ingelheim (Ridgefield, CT)
- …management activities to BI decision making bodies and the EU QPPV + Represent Global Pharmacovigilance in internal and external committees & bodies. This may ... global Inflammation Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or… more
- Boehringer Ingelheim (Ridgefield, CT)
- …activities to BI decision making bodies and the EU QPPV. + Represent Global Pharmacovigilance in internal and external committees & bodies. + Contribute ... global Oncology Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...hired_** **_at level commensurate with experience and education._** **Sr. Associate Director Requirements:** + US MD or… more
- AbbVie (South San Francisco, CA)
- …LinkedIn. Job Description In collaboration with a therapeutic area, the Scientific Director , Clinical Science will lead the design, conduct, analysis, and reporting ... medical education strategy for late-stage assets. + May oversee the work of Associate Scientific Directors and/or of Clinical Scientists working on the same or… more
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