- Amgen (Washington, DC)
- … safety / pharmacovigilance experience OR Bachelor's degree and 6 years of safety / pharmacovigilance experience OR Associate degree and 10 safety / ... with these qualifications. **Basic Qualifications:** Doctorate degree and 2 years of safety / pharmacovigilance experience OR Master's degree and 4 years of… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …or + RN degree preferred **Experience Qualifications** + 4 or More Years drug safety experience with technical experience in Electronic Data Capture and ... industry experience in one or more of the following areas: Drug Safety , Epidemiology, and Clinical Development preferred Daiichi Sankyo, Inc. is an… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …clinical research, or other related healthcare environment, including significant experience working in drug safety /PV or a related field OR + MA/MS/MBA in life ... a highly motivated individual to join us as an Associate Director, Patient Safety Risk Management. Under...other related healthcare environment, including significant experience working in drug safety /PV or a related field will… more
- Ascendis Pharma (Palo Alto, CA)
- …Key Responsibilities . Assists Head of Global Medical Safety Science for drug safety and pharmacovigilance activities for ensuring corporate compliance ... workplace for employees to grow and develop their skills. Associate Director, Medical Safety Science reports to...Safety Science, is responsible for all assigned Ascendis Drug Safety PV related activities for all… more
- Boehringer Ingelheim (Ridgefield, CT)
- …or coach direct reports to provide updates of the assigned drug 's safety profile to senior management and recommend pharmacovigilance / risk management ... team of physicians in the global Cardio-metabolism/Respiratory Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing… more
- Boehringer Ingelheim (Ridgefield, CT)
- …review of team output. + Provide updates of the assigned drug 's safety profile to senior management and recommend pharmacovigilance / risk management ... and expert team of physicians in the global Oncology Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of our… more
- United Therapeutics (Columbus, OH)
- …aspects of drug development & registration of medicines, ensuring their safety + Strong analytical thinking to diagnose common situations, gather and review ... and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Associate Global PV Case Management Director plays a key role in management… more
- System One (Jersey City, NJ)
- …Manager, Project Management is responsible for providing support to regional and global Drug Safety Pharmacovigilance (PV) projects. Projects include global ... Notes: Seeking someone with project management experience and has working knowledge of Drug Safety , MS Project and MS Excel. POSITION OVERVIEW/SUMMARY The Senior… more
- AbbVie (Jersey City, NJ)
- …signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities. Experts on ... toxicology to effectively conduct safety surveillance + Responsible for safety surveillance for pharmaceutical / biological / drug -device combined… more
- Takeda Pharmaceuticals (Boston, MA)
- …the cross-functional interfaces with key partners such as Pharmacometrics, Statistics, Drug Safety , Clinical Sciences, Outcomes, Digital Health, Pharmaceutical ... clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance , digital strategy, library sciences and… more
- Lilly (Indianapolis, IN)
- …in its process, standards, procedures and behaviors to develop medicines with safety first and quality always **Position Brand Description:** The Sr. Principal ... Associate - Quality Due Diligence Assessment Auditor (QDDA) is...of pharmaceutical development, non-clinical and clinical research, product commercialization, pharmacovigilance and consumer information quality (CIQ) for Lilly. Through… more
- AbbVie (North Chicago, IL)
- …2+ years patient care experience strongly preferred + Minimum 2 years' experience in drug safety or a related discipline in the pharmaceutical industry + ... to pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans + Contribute to… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …medical coding services for assigned programs, collaborating with program teams, clinical safety and pharmacovigilance , CROs, and partners to ensure high quality ... coding deliverables are on time to support drug development processes and global submissions. This position also...working knowledge of medical terminology capture and reporting of safety data, pharmacovigilance , industry best practices, and… more
- Bausch + Lomb (Rochester, NY)
- …Person for consumer-related issues escalated by team members + Manage communication within Drug Safety ( Pharmacovigilance ) email box + May collaborate with ... respond to the post or answer any questions: Regulatory- Pharmacovigilance , R&D, all other Bausch + Lomb sites worldwide,...use preferred and 1 year customer service experience + Associate or Bachelor's Degree preferred + Experience with the… more
- AbbVie (North Chicago, IL)
- …integrity and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... limited supervision, for the proactive monitoring of clinical trial safety which is conducted in collaboration with the ABV...issues and queries. + May oversee the work of Associate Medical and/or Scientific Directors and of Clinical Scientists… more
- AbbVie (South San Francisco, CA)
- …training and clinical research experience to support all aspects of drug development, from facilitating the transition of molecules from pre-clinical discovery ... and communication of scientific data pertaining to the efficacy and safety of compounds in development. Attends conferences, reviews medical literature and… more
- AbbVie (Irvine, CA)
- …integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... submissions and responses and other program documents. *May oversee the work of Associate Scientific Directors and/or of Clinical Scientists working on the same or… more
- AbbVie (North Chicago, IL)
- …integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... 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… more
- AbbVie (North Chicago, IL)
- …integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... 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… more
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