- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …rare diseases and immune disorders. **Summary** This position works with the Director , Clinical Study Startup to establish the strategy driving global Clinical Study ... Start-Up activities for PV Safety Operations. This position oversees the creation of SAE...where appropriate and escalate any complex problems to the Director , Clinical Study Startup. This position requires strong organization… more
- AbbVie (North Chicago, IL)
- …opportunities. The Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety leads the scientific strategy for pharmacoepidemiology ... and real-world evidence to support product development and safety across therapeutic areas. They will design and interpret studies, contribute to regulatory… more
- AbbVie (Chicago, IL)
- …Description The Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety leads the scientific strategy for pharmacoepidemiology and ... real-world evidence to support product development and safety across therapeutic areas. They design and interpret studies, contribute to regulatory submissions, and… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …in this 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), you are responsible for contributing to the initiation, management, and execution of key… 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 ... of Global Medical Safety Science for drug safety and pharmacovigilance activities for ensuring corporate...team (specifically from: Talent Acquisition Partner or Human Resources Director ) is not allowed. If this occurs your ownership… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …of systems, configuration and associated validation activities of Daiichi Sankyo Pharmacovigilance Safety systems, and fulfillment of data change requests. ... process improvements. + Provide oversight, Manage Implementation and documentation of PV Safety systems Change Request supporting documents and evidence + Review of… more
- Novo Nordisk (Plainsboro, NJ)
- …to the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring ... and other key internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing relationships with internal… more
- United Therapeutics (Columbus, OH)
- …cardiovascular and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Associate Global PV Case Management Director plays a key role in ... management and oversight of end-to-end case safety management activities spanning across our global commercial product portfolio. This position strategizes and… more
- ThermoFisher Scientific (Carlsbad, CA)
- …to 1-2 years) in the industry; Or + Direct experience in safety / Pharmacovigilance (comparable to 2 years) Medical Director level requires: + Clinical ... (comparable to 1-2 years) in the industry; Or + Direct experience in safety / Pharmacovigilance (comparable to 2 years). **Qualified candidates should have a… more
- Novo Nordisk (Plainsboro, NJ)
- …grows. Relationships Reports to the Sr. Director , Patient Support Solution Quality/ Safety Associate Director . Interacts with colleagues within Patient ... to maximize your potential with us? The Position The Associate Director will be the lead who...Understanding of regulatory requirements and guidelines related to patient safety , pharmacovigilance and pharmaceutical operations + Excellent… 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
- AbbVie (Jersey City, NJ)
- …signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Experts on ... pharmacy, clinical development, and discovery + Works closely with Executive Medical Director to establish safety strategy for each indication and across… more
- Takeda Pharmaceuticals (Boston, MA)
- …Lead CPMQ continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and support to the ... CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and ensure key… 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 ... to our inspiring, bold mission **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy...assessing issues related to protocol conduct and/or individual subject safety . + Assesses overall safety information for… 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 ... physicians in the global Oncology Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority...and more than 3 years of applicable experience, required. ** Director Requirements:** + US MD or DO degree or… more
- AbbVie (North Chicago, IL)
- …Group Medical Director to develop of best practices in patient safety across innovative trials, support platform program teams and help ensure that appropriate ... to pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans + Contribute to… 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 ... clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance , digital strategy, library sciences and… 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 ... clinical trials and safety evaluation within the Pharmacovigilance department. **A day in the Life:** + Provide medical leadership to the study teams, including… more
- AbbVie (North Chicago, IL)
- …core R&D sub-functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance , Medical Affairs, Regulatory Affairs, and Clinical Development (both ... review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Partner with Clinical...+ Participate in design and execution of clinical trial safety , product safety , and risk management plans.… more
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