- Astrix Technology (Chicago, IL)
- ** Drug Safety Physician ** Clinical Chicago, IL,...is preferred. + Minimum of 3 years of experience in pharmacovigilance or drug safety within the ... range of clients across various industries. We're seeking talented Drug Safety Physicians to join us! Our...to health authority inquiries. + Stay current with global pharmacovigilance regulations and guidelines to ensure compliance and best… more
- Lilly (San Diego, CA)
- …and relevant therapeutic area experience , the Early Development Clinical Research Physician participates in the following: the development, conduct and reporting of ... and the reporting of adverse events as mandated by corporate patient safety ; the generation and review process for protocols, study reports, publications and… more
- J&J Family of Companies (Titusville, NJ)
- …Licensing & Acquisition opportunities + Provide medical oversight to contractors and non- physician staff involved in preparing written safety evaluations for ... pharmacology, clinical trial methodology and design, medical monitoring of trials, assessment of drug risks and benefits, and safety assessment of drugs both on… more
- ThermoFisher Scientific (Greenville, NC)
- …globally to support training and end to end medical monitor and/or safety physician activities and supporting services across the pharmaceutical product ... maybe required). **Discover Impactful Work:** Advanced leadership responsibilities within the Pharmacovigilance (PV) physician team which may include direct line… more
- Pfizer (New York, NY)
- …medicine, specialty training and/or board certification), and/ or scientific, and/or pharmacovigilance or and/or drug development Additional Qualifications + ... development process and post-marketing experience, including and understanding of safety context across the drug lifecycle +...the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of… more
- Takeda Pharmaceuticals (Boston, MA)
- …activities, assessing issues related to protocol conduct and/or individual subject safety . Assesses overall safety information for studies and products ... in conjunction with Pharmacovigilance . Oversees non-medical clinical scientists with respect to assessment...specialty is desired. + 3-5 years of strong clinical research/ drug development experience within the pharmaceutical industry is required.… more
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