Browse 31 exciting jobs hiring in Pharmacovigilance now. Check out companies hiring such as Pfizer, AbbVie, Advanced Technology Services in St. Petersburg, Honolulu, Dallas.
Support Pfizer’s safety surveillance by processing and assessing adverse event reports and ensuring regulatory-compliant pharmacovigilance across clinical and post-marketing programs.
AbbVie is hiring an Associate Director for RBQM Analytics to lead analytics strategy, grow talent, and deploy advanced analytics across clinical quality and risk-management functions.
Provide strategic leadership and hands‑on medical affairs support for AbbVie's intercontinental neuroscience portfolio, driving evidence generation, affiliate training, and cross‑functional collaboration for Parkinson's and migraine assets.
Senior leader sought to direct and scale global pharmacovigilance operations, optimizing quality, speed and cost while ensuring regulatory compliance across regions.
AbbVie is hiring an Associate in Support Operations to accurately register and process adverse event reports and maintain regulatory-compliant pharmacovigilance data while working remotely with monthly travel to Lake County, IL.
Experienced clinician-scientist needed to lead obesity-focused clinical development programs, guiding protocol design, safety strategy, and regulatory interactions at Regeneron’s Tarrytown site.
Lead a team of epidemiologists to deliver high-quality observational research and causal-inference analyses that inform product safety, regulatory strategy, and clinical decision-making at Amgen.
Immunovant seeks an experienced Senior Director, Clinical Operations to lead global clinical trial operations, vendor strategy, and cross-functional execution for a development asset in a dynamic, fast-paced biotech environment.
AbbVie seeks a Clinical Safety Analyst to perform safety surveillance, SAE narrative creation, and study-level safety reviews for clinical trials while collaborating with medical monitors and clinical teams.
Experienced neuroscience medical affairs leader needed to drive regional medical strategy, evidence generation, and affiliate support for AbbVie's neuroscience assets from the Mettawa, IL hybrid site.
Takeda is seeking an Associate Director to lead clinical and safety quality compliance activities, ensuring regulatory alignment, audit readiness, and implementation of process improvements across global clinical and pharmacovigilance operations.
Experienced pharmacovigilance operations leader wanted to manage and develop Support Operations teams, ensuring efficient case initiation, data entry and documentation in support of drug safety and regulatory compliance.
Experienced, board-certified veterinary anatomic pathologist needed to lead pathology for in vivo studies, GLP reporting, and translational safety science at Zoetis in Kalamazoo (hybrid, 50% onsite).
Experienced oncology physician needed to join a global medical affairs team as Senior Medical Monitor, providing medical oversight, safety review, and medical input for clinical studies.
Deciphera is hiring a Senior Director, Pharmacovigilance Sciences to lead PV Sciences, drive safety strategy and regulatory safety deliverables across the portfolio.
AbbVie is recruiting a Medical Director / Senior Medical Director to lead clinical development programs in North Chicago, providing medical leadership for protocol design, safety oversight, and regulatory interactions.
Experienced physician with clinical trial expertise sought to lead immunology clinical development programs and provide medical leadership at AbbVie.
AbbVie is seeking an Associate Director to lead quality assurance for Medical Affairs and RWE activities, ensuring regulatory compliance and driving quality strategies across drug, device, and cosmetic portfolios.
Lead and manage the Support Operations team within GCM Clinical Case Management to ensure accurate, compliant pharmacovigilance operations and continuous process improvement.
Lead and optimize global pharmacovigilance processes at Bristol Myers Squibb, ensuring regulatory inspection readiness, process governance, and continuous improvement.
Experienced physician with pharmacovigilance and clinical development background needed to lead product safety teams and oversee safety strategy for oncology and specialty products at AbbVie.
AbbVie is hiring a Group Medical Director, Patient Safety to lead safety strategy and teams for its late-stage and post-marketing solid tumor oncology portfolio at the North Chicago site.
AbbVie is hiring an MD/DO to lead pharmacovigilance and product safety teams for oncology and specialty products, overseeing signal detection, safety assessments and risk management across development and marketed phases.
AbbVie is hiring a Lead Principal Medical Safety Analyst to lead vendor oversight for pharmacovigilance case processing and ensure compliant, high-quality adverse event management.
Deciphera is hiring a Medical Director, Pharmacovigilance to lead medical safety review, signal evaluation and benefit-risk activities for oncology products from the Waltham office.
Experienced clinical development leader needed to design and drive oncology study protocols and cross‑functional execution at AbbVie in North Chicago.
Lead AbbVie's hematology-oncology safety strategy as Group Medical Director, overseeing PV teams, aggregate safety assessments, and cross-functional safety decisions for late-stage and post-marketing assets.
AbbVie is hiring a Medical Director to lead product safety teams and drive pharmacovigilance strategy for pharmaceutical, biological, and drug–device combination products.
Experienced physician with pharmacovigilance expertise needed to support and potentially lead product safety surveillance, signal detection, and risk management for AbbVie's immunology portfolio.
Entry-level physician leaders (Associate Medical Directors) are sought for a two-year, onsite rotational Physician's Development Program at AbbVie's North Chicago R&D headquarters to gain cross-functional clinical development experience in oncology and related therapeutic areas.
Physician-level safety expert needed to evaluate translational immunology data, support safety lead activities, and author early development safety documents at AbbVie in North Chicago.
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