Pharmacovigilance Jobs

Experienced physician needed to serve as Medical Director at a collaborative CRO, providing medical oversight, safety review, and scientific guidance across clinical programs.

AbbVie is recruiting a Safety Deliverable Manager to drive and author PST safety deliverables, ensuring high-quality, regulatory-compliant safety summaries and aggregate reports across product lifecycles.

Senior physician to lead oncology clinical development programs, driving trial design, safety oversight and medical strategy across GSK's oncology portfolio.

Lead a Medical Information contact center client portfolio at EVERSANA, combining clinical expertise (PharmD) with team leadership, client management, and medical writing to deliver compliant, high-quality responses.

Eurofins is hiring a remote Pharmacovigilance Specialist (DVM) to drive post‑marketing safety surveillance, signal detection, and provide PV expertise across product lines.

Lead global contact center and medical information operations at Moderna to ensure compliant, high-quality engagement for patients and healthcare professionals while scaling capabilities for a growing pipeline.

Lead strategic regulatory labeling activities for AbbVie’s US/EU products, coordinating cross-functional teams to ensure compliant, consistent and optimized product labeling.

Experienced vaccines clinical scientist to lead program-level clinical design, scientific oversight, and cross-functional execution for global studies at Pfizer.

Orchard Therapeutics seeks an experienced VP of Clinical Development to lead global clinical science, design and execute clinical strategies, and represent clinical development in regulatory and cross-functional engagements for its gene therapy programs.

Experienced medical writer needed to author and QC safety sections of Phase I/II clinical study reports for a US-based, remote role at Celerion.

argenx is hiring a Nurse Case Manager in New York City to provide clinical education, care coordination and reimbursement support to patients with gMG as their primary patient-facing clinical contact.

Senior physician leader responsible for setting and executing safety strategy for AbbVie's late-stage solid tumor oncology portfolio while mentoring and directing the oncology safety team.

AbbVie seeks specialist physicians (MD/DO) for a two-year Physician Development Program based in North Chicago to develop clinical research and medical affairs expertise through rotational assignments across R&D functions.

Senior medical affairs leader needed to shape oncology brand strategy, drive evidence generation and clinical support, and partner cross-functionally to advance AbbVie’s hematology/oncology portfolio.

AbbVie seeks early-career physician specialists to participate in a two-year onsite Physician Development Program in North Chicago, rotating through core R&D functions as Associate Medical Directors.

Syneos Health is hiring a Principal Biostatistician to lead safety surveillance and RWE analyses across North America, providing statistical leadership and regulatory-ready deliverables.

A two-year onsite rotational program at AbbVie’s North Chicago HQ that develops specialist physicians into Associate Medical Directors through cross-functional R&D rotations in oncology and related therapeutic areas.

Experienced oncology medical affairs leader needed to drive scientific strategy, clinical evidence generation, medical education, and safety oversight for AbbVie’s hematology/oncology programs on a hybrid schedule based in Mettawa, IL.

AbbVie's two-year Physician Development Program prepares recent M.D./D.O. specialists for R&D careers through rotational assignments across clinical development, safety, regulatory and medical affairs at the North Chicago headquarters.

AbbVie’s two-year Physician Development Program prepares graduating fellows for careers in R&D by providing onsite rotations and mentorship across clinical development, safety, medical affairs and regulatory functions.

AbbVie seeks M.D./D.O. candidates (recent residency or fellowship graduates) for a two-year, onsite Physician Development Program in Neuroscience and related therapeutic areas, entering as Associate Medical Directors to gain cross-functional R&D experience.

Senior medical writer and team lead role responsible for authoring regulatory submissions and maturing medical writing processes at a growth-stage biotech focused on immunology.

AbbVie is hiring Associate Medical Directors for a two-year onsite Physician’s Development Program in North Chicago, focused on developing fellows into R&D medical leaders across clinical development, safety, regulatory, and medical affairs.

AbbVie is looking for an experienced Medical Director to lead product safety teams and drive pharmacovigilance strategy across clinical and marketed products.

Experienced physician-leader wanted to drive neuroscience clinical development at AbbVie, owning protocol design, safety oversight, and cross-functional clinical strategy for complex programs.

AbbVie is hiring an Associate Medical Director/Medical Director to lead oncology clinical development activities, including protocol design, safety oversight, and cross-functional scientific strategy.

Senior PV leader needed to drive operational excellence, program delivery, and regulatory-ready processes for Novartis' US pharmacovigilance organization.

Lead clinical development strategy and execution for hematology programs at AbbVie, providing medical and scientific leadership across global cross-functional teams.

Ro is hiring a Quality & Safety Manager to lead clinical incident investigations, safety monitoring, and risk assessment across its nationwide telehealth and pharmacy platform.

AbbVie is hiring a Medical Director in Neuroscience Clinical Development to lead clinical strategy, study design and safety oversight for CNS programs at its North Chicago campus.

PrimeVigilance is hiring a detail-oriented PV Assistant in Raleigh to support ICSR handling, safety message management, and routine pharmacovigilance documentation with training provided.

Senior clinical leader needed to drive clinical strategy, study design, safety oversight, and regulatory documentation for Kyverna’s cell- and gene-therapy programs in a remote capacity.

Harrow seeks a remote Pharmacovigilance Data Entry Associate to accurately document and triage inbound medical inquiries, PQCs and AE reports for the MICC.

AbbVie is looking for an experienced Group Medical Director to lead safety strategies and teams for their hematology-oncology product portfolio.

Ascendis Pharma seeks a contract-experienced ICSR Lead to oversee safety report processing and compliance in their Global Patient Safety organization.

Experienced board-certified neurologist needed to provide expert medical monitoring for global clinical studies with PSI, a top CRO.

Seeking a skilled GVP Auditor specialized in Postmarketing Surveillance and PADE Inspections to join ProPharma for a four-day onsite audit in Italy.