Pharmacovigilance

495 open positions

Senior Manager PV Sweden & Affiliate Safety Representative ViatrisSolna, Stockholm County, Sweden 4mo Organize, manage, and maintain a highly compliant Pharmacovigilance (PV) system for Viatris in Sweden, acting as the main contact for health authorities and leading the local PV team.
Senior Consultant Pharmakovigilanz / Life Sciences (m/w/d) DeloitteDüsseldorf 4mo Develop innovative regulatory and compliance solutions for Life Sciences clients, focusing on Pharmakovigilance (PV) to improve processes, organizational structures, and IT systems.
Senior Drug Safety Associate IconBulgaria, Sofia 4mo Managing and overseeing pharmacovigilance activities to ensure the safety and efficacy of pharmaceutical products, including adverse event reporting and signal detection.
Medical Director/Sr Medical Director - Rheumatology ThermofisherRemote, Argentina 4mo Provides medical oversight of clinical trials and marketed products to ensure regulatory compliance and safety, serving pharmaceutical clients and biotech partners.
Pharmacovigilance Associate Position Puma Biotechnology, Inc.Los Angeles, Los Angeles, California, United States 4mo Process adverse events and special situation cases to ensure timely, accurate, and compliant Individual Case Safety Report (ICSR) intake, processing, reporting, and reconciliation.
Senior Manager Medical Review RegeneronHyderabad 4mo Lead medical review of safety cases to ensure scientific soundness and inspection readiness for health authority submission.
Clinical Safety Coordinator Entry - (Fresh nursing graduates) MedpaceNavi Mumbai, India 4mo Entry-level Clinical Safety/Drug Safety Coordinator managing adverse event reporting and safety narratives for clinical trials.
Drug Safety Specialist/ Clinical Safety Coordinator MedpaceNavi Mumbai, India 4mo Handling and processing adverse events from clinical trials and post-marketing surveillance sources.
Clinical Safety Coordinator - Pharmacovigilance (Nursing Professionals Encouraged to Apply) MedpaceSeoul, Korea, South 5mo Full-time Clinical Safety Coordinator supporting pharmacovigilance operations and regulatory reporting in South Korea.
Associate Director, Triage and Medical Review RegeneronHyderabad 5mo Lead triage and medical review of Individual Case Safety Reports (ICSRs) for global development programs and marketed products, ensuring quality and alignment with pharmacovigilance standards.
Director, Global Patient Safety Sciences - General Medicine RegeneronCambridge, MA, US $205k5mo Lead global patient safety strategy, signal management, and regulatory compliance for assigned compounds in general medicine.
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Oncologist↗ Remote $728k5mo Evaluate AI-generated oncology clinical outputs for reasoning, dosing, and guideline adherence to ensure patient safety.
Medical Monitor (Gastroenterologist) Psi-CroRemote 5mo Provides medical input to global clinical studies, focusing on patient safety, regulatory interactions, and therapeutic expertise in gastroenterology.
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Computational Chemistry & Drug Discovery Scientist (PhD) — AI Evaluation↗ Remote 5mo Evaluate AI outputs for clinical reasoning, dosing logic, and guideline adherence in drug discovery workflows to ensure patient safety and model accuracy.
Pharmacovigilance (PV) Director, Japan GehcJPN55-01-Tokyo-WeWork Shinagawa PDx, JP 6mo Senior leadership role ensuring safe and compliant commercialization of pharmaceutical products in Japan, serving as the Anseki (Safety Management Supervisor) and primary interface with PMDA.
Medical Director/Sr Medical Director - Neurology(Remote U.S) ThermofisherRemote 6mo Provide medical oversight of clinical trials and marketed products for top pharmaceutical and biotech clients, ensuring adherence to GCP, regulatory requirements, and client directives.
Drug Safety Associate (Life Sciences Degrees) MedpaceCincinnati, Ohio 7mo Collect, process, and track serious adverse event (SAE) reports; generate safety narratives and queries; perform quality control of safety cases.
Clinical Safety Nurse MedpaceCincinnati, Ohio 7mo Handling and processing adverse events from clinical trials and post-marketing surveillance sources.
Clinical Safety Manager MedpaceCincinnati, Ohio 7mo Lead clinical safety operations and pharmacovigilance activities for clinical trials, ensuring high-quality case management and reporting for clients.
Medical Information Specialist - German & English speaking EversanaRemote 7mo Respond to drug information inquiries from healthcare professionals and patients, manage adverse event reporting, and perform medical writing.
Solution Consultant - Veeva Safety VeevaRemote €80k–€150k7mo Bridge complex pharmacovigilance challenges with Veeva's Vault Safety cloud solutions to help life sciences companies streamline safety processes.
Pharmacovigilance Associate II BmsWarsaw-WeWork-PL 105k8mo Coordinate crucial pharmacovigilance activities, manage a Book of Work of increased complexity, and mentor colleagues to support global drug development projects.
Senior Pharmacovigilance Associate BmsWarsaw-WeWork-PL 118k8mo Provide strategic and operational support for signal detection, safety data review, and risk management across therapeutic areas to advance drug safety.
Solution Consultant - Safety VeevaRemote $80k8mo Bridge complex pharmacovigilance challenges with Veeva's Vault Safety cloud solutions to help Life Sciences companies unify their safety processes.
Senior Safety Physician CatalymCatalYm GmbH 9mo Lead strategic direction for Clinical Drug Safety, overseeing safety profile evaluation and implementing safety standards for clinical development programs.
Regulatory Affairs Officer Ghobash-GroupDubai, Dubai, ae 9mo Managing pharmaceutical, veterinary, and medical product registrations and liaising with regulatory authorities to obtain approvals.
Medical Information Specialist I (Pipeline / Fluent in English & Spanish Only) ThermofisherSão Paulo, Brazil 10mo Provides technical and medical information and manages intake of adverse events/product complaints for pharmaceutical and device products.
Medication Safety Analyst DeloitteImo State, ng 11mo Monitor, analyze, and report on medication use and safety incidents to identify trends, evaluate risks, and provide actionable insights to improve patient safety and reduce medication errors.
Med Info Assoc I (Pipeline) ThermofisherMexico City, Mexico 1y Provides technical and medical information, manages intake of adverse events and product complaints, and supports clinical trial information for pharmaceutical or device products.
Medical Information Specialist I (Pipeline) ThermofisherSão Paulo, Brazil 1y Provides technical and medical information and manages intake of adverse events/product complaints for pharmaceutical or device products.
Medical Affairs Manager - Pharmakovigilanz (m/w/d) Hameln Pharma GMBHRemote 1y Provide drug information for Hameln products in response to medical/pharmaceutical inquiries from the German/Austrian professional community and support the creation and review of aggregated safety reports (PSURs, PBRERs).
Pharmaziepraktikant*in Medical Affairs & Pharmakovigilanz für 2027 (alle Geschlechter) BayerBerlin,Berlin,Germany €27k1y Pharmacist intern gaining exposure to drug safety monitoring, adverse event collection, and benefit-risk profiling within a global pharmaceutical company.
(Associate) Medical Director - Neurology ThermofisherRemote, Portugal 1y Provide medical leadership and safety evaluation for clinical trials in the Pharmacovigilance department, focusing on neurology and epilepsy.
Chile_Technical Manager CelltrionhealthcareSantiago, CL 1y Manage product registration, regulatory compliance, and pharmacovigilance for biosimilar and innovative biopharmaceutical medications in Chile.
Consultant - Veeva Safety - Managed Services (Remote) VeevaRemote 1y Drug Safety and Pharmacovigilance consultant supporting Veeva Vault Safety implementation and post-implementation managed services for biopharmaceutical customers.
Global Head of Clinical Safety GaldermaBarcelona 1y Providing medical safety expertise for benefit/risk assessment of products in clinical development, specifically for the biologic Nemolizumab, including signal detection, risk management, and safety analyses.
Senior Consultant - Pharmacovigilance/Safety Systems Implementation (Remote) VeevaRemote $80k1y Lead implementations of Vault Safety solution for life sciences customers, defining business processes and guiding project delivery.
Consultant - Vault Safety VeevaRemote 2y Implement and configure Vault Safety solutions for life sciences customers, bridging the gap between existing safety systems and Veeva's platform.
Senior Consultant - Veeva Safety - Managed Services (Remote) VeevaRemote 240k–380k4y Senior Consultant leading rapid configuration and implementation of Vault Safety for pharmaceutical customers, ensuring alignment of drug safety processes with system design.
Consultant - Veeva Safety - Managed Services (Remote) VeevaRemote 12000k–23000k4y Support Veeva Vault Safety solution for biopharmaceutical customers post-implementation, guiding adoption of industry best practices and driving change management from on-premises to SaaS.
Consultant - Veeva Safety - Managed Services (Remote) VeevaRemote 160k–265k4y Support Veeva Vault Safety solution for biopharmaceutical customers post-implementation, guiding them on configuration, best practices, and change management.
Consultant - Pharmacovigilance/Safety Systems Implementation (Remote) VeevaRemote $80k4y System implementation expert for Vault Safety solution, guiding life sciences customers through configuration, gap analysis, and business process definition.
Senior Implementation Consultant – Pharmacovigilance / Safety Systems (Remote) VeevaRemote 4y Senior consultant driving the configuration, implementation, and delivery of Vault Safety solutions for life sciences customers, acting as Project Manager and/or Solution Architect.
Director - Vault Safety Suite VeevaRemote $125k5y Driving market adoption and customer success for Veeva's Vault Safety Suite in the life sciences industry within the Northeast US.
About the job SK GroupSK플라즈마 판교 본사 Managing active monitoring of Pharmacovigilance (PV) and Post-Marketing Surveillance (PMS) activities in compliance with Risk Management Plans (RMP), including managing investigation agencies and CROs, reviewing and approving reports, and updating regulatory…

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