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Healthcare
› Pharmacovigilance
Pharmacovigilance
356 open positions
Safety Physician
Tata Consultancy Services
India
3mo
Provides scientific and medical expertise in Safety Evaluation and Risk Management (SERM) across clinical development and post-marketing products, ensuring robust safety assessment, signal detection, and regulatory compliance.
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(Senior) Patient Safety Physician - Inflammation
Boehringer Ingelheim GmbH
Ingelheim am Rhein, Mainz-Bingen (Kreis)
3mo
Lead global Patient Safety and Pharmacovigilance (PSPV) and Risk Management activities for compounds in clinical development and post-marketing phases, focusing on inflammatory diseases.
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(Senior) Patient Safety Physician CRM
Boehringer Ingelheim GmbH
Ingelheim am Rhein, Mainz-Bingen (Kreis)
3mo
Lead or contribute to integrated Patient Safety and Pharmacovigilance (PSPV) activities for compounds in clinical development or post-marketing, focusing on cardiovascular, renal, hepatic, and metabolic diseases.
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Senior Manager Medical Review
Regeneron
Hyderabad
3mo
Lead medical review of safety cases to ensure scientific soundness and inspection readiness for health authority submission.
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Senior Physician, Patient Safety
Parexel
India
3mo
Senior medical expert performing complex case reviews, causality assessment, and regulatory compliance for adverse event reporting in clinical trials.
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Local Contact Person for Pharmacovigilance - LCPPV in France (Freelance)
Tepsivo
Remote
3mo
Support customers with local pharmacovigilance system implementation and maintenance in France, including regulatory intelligence and audit support.
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Pharmacovigilance Project Manager
Ire
São Paulo, Estado de São Paulo
3mo
Leading and overseeing pharmacovigilance activities across clinical trials and post-marketing studies to ensure drug safety and regulatory compliance.
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Pharmacovigilance Project Manager
ICON Clinical Research
São Paulo, Estado de São Paulo
3mo
Leading and overseeing pharmacovigilance activities for post-marketing projects and clinical trials, ensuring regulatory compliance and safety monitoring.
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PV Physician-Medical Assessment
Dr Reddys
Hyderabad, Telangana
3mo
Oversight of medical input to benefit-risk assessment activities, including signal detection, evaluation, and risk management plan development.
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Executive Director, Global Patient Safety Sciences Delivery
Regeneron
Uxbridge1
3mo
Lead global operations and risk management for patient safety sciences, ensuring consistency in safety surveillance, signal detection, and regulatory reporting across all therapeutic areas.
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alternance 12 mois - science en pharmacovigilance
Sanofi Group
Gentilly, L'Haÿ-les-Roses
3mo
Participate in the surveillance of product safety for clinical development or marketed products within the Global PV Science team.
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Associate Director, Triage and Medical Review
Regeneron
Hyderabad
3mo
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.
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VP, Global Patient Safety Sciences, General Medicine
Regeneron
TARRYTOWN
3mo
Define global patient safety strategy for general medicine assets, lead clinical risk assessment, and provide scientific oversight for safety signals and benefit-risk evaluations.
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Director, Global Patient Safety Sciences - General Medicine
Regeneron
Cambridge, MA, US
$205k–$205k
3mo
Lead global patient safety strategy, signal management, and regulatory compliance for assigned compounds in general medicine.
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Medical Director/Senior Director
Eversana
India
3mo
Leading a team of scientists and physicians to manage aggregate safety reporting, signal detection, and regulatory compliance for multiple client programs.
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Medical Monitor (Gastroenterologist)
Psi-Cro
Remote
3mo
Provides medical input to global clinical studies, focusing on patient safety, regulatory interactions, and therapeutic expertise in gastroenterology.
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Senior Safety Physician
CatalYm GmbH
Planegg, München (Kreis)
3mo
Lead strategic direction for Clinical Drug Safety, overseeing safety profile evaluation and implementing safety standards for clinical development programs.
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Executive Director, Global Patient Safety Sciences - Rare Disease
Regeneron
TARRYTOWN
$286k–$286k
3mo
Define product safety strategy and provide medical safety opinion for the Rare Disease portfolio across clinical and post-marketed drugs.
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Pharmacovigilance Specialist Italy
Biomapas
Remote
3mo
Local Safety Officer and Medical Information Specialist ensuring compliance with Italian pharmacovigilance regulations and managing safety information flow.
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Director, Safety Physician
Summit Therapeutics
UK
$0k–$0k
3mo
Director of Safety Physician leading medical review of individual case safety reports (ICSRs), signal detection, and aggregate safety reporting for oncology investigational and marketed products.
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Senior Safety Committee Specialist - Adjudication
Thermofisher
Remote, Mexico
3mo
Lead complex safety projects and ensure successful implementation of pharmacovigilance practices for Clinical Evaluation Committees (CEC) and Data and Safety Monitoring Boards (DSMB).
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Biotech Investment Analyst — Drug Asset & Company Assessment Review
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Remote
$250k–$250k
3mo
Evaluate AI-generated clinical outputs for drug asset assessments by grading reasoning, dosing logic, and guideline adherence to ensure patient safety and model improvement.
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Manager, Drug Safety Physician
World Courier
Noida, Ghaziabad
4mo
Conduct medical reviews of individual case safety reports (ICSRs), screen scientific literature for safety signals, and prepare periodic safety reports.
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Italy_Medical Information Specialist & PV Officer
Celltrion Group
Milano, Provincia di Milano
4mo
Providing scientific and medical information to healthcare professionals and patients while managing adverse event reporting and safety data for biosimilar and biopharmaceutical products.
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Pharmacovigilance - Project Manager
Med Communications International
Warszawa, mazowieckie
4mo
Senior client-facing professional managing end-to-end operational delivery of pharmacovigilance services including case management, periodic reporting, signal detection, and risk management.
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Medical Director/Sr Medical Director - Cardiology(Remote)
Thermofisher
Remote
4mo
Provide medical oversight of clinical trials and marketed products, ensuring compliance with regulations and client directives while managing safety data and therapeutic expertise.
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Pharmacovigilance (PV) Director, Japan
Gehc
JPN55-01-Tokyo-WeWork Shinagawa PDx, JP
4mo
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.
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Medical Safety Physician
Diensten Tech Limited
Gurgaon, Haryana
5mo
Ensuring patient safety and compliance with regulatory requirements for products through medical safety strategies and risk management.
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Pharmacovigilance Specialist France
Biomapas
Remote
5mo
Local Safety Officer and Medical Information Specialist ensuring compliance with French pharmacovigilance regulations and managing safety information flow.
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Medical Director/Sr Medical Director - Neurology(Remote U.S)
Thermofisher
Remote
5mo
Provide medical oversight of clinical trials and marketed products for top pharmaceutical and biotech clients, ensuring adherence to GCP, regulatory requirements, and client directives.
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Clinical Research Associate - NSW
Novotech
The Rocks, Sydney
5mo
Provide medical oversight for clinical trials, including protocol review, safety assessment, and data interpretation.
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Senior Director, Responsible Pharmacist (Pharmacien Responsable), France
Revolution Medicines
France
5mo
Senior Director ensuring pharmaceutical responsibility and regulatory compliance for a late-stage oncology company's drug manufacturing, distribution, and safety operations in France.
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PV Manager Safety Science
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Thermo Fisher Scientific
Remoto, PT
5mo
Manages the safety profile of new drugs in clinical trials, overseeing case-processing, regulatory reporting, and medical monitoring for a multinational team.
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Medical Information Specialist - German & English speaking
Eversana
Remote
5mo
Respond to drug information inquiries from healthcare professionals and patients, manage adverse event reporting, and perform medical writing.
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Solution Consultant - Veeva Safety
Veeva
Remote
$80k–$150k
6mo
Bridge complex pharmacovigilance challenges with Veeva's Vault Safety cloud solutions to help life sciences companies streamline safety processes.
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Solution Consultant - Safety
Veeva
Remote
$80k–$80k
6mo
Bridge complex pharmacovigilance challenges with Veeva's Vault Safety cloud solutions to help Life Sciences companies unify their safety processes.
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Senior Consultant - Veeva Safety Project Management
Veeva
Remote
6mo
Lead global teams to implement Veeva Vault Safety solutions for biopharmaceutical customers, managing the full lifecycle from discovery to Go-Live.
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Regulatory Affairs Officer
Ghobash-Group
Dubai, Dubai, ae
7mo
Managing pharmaceutical, veterinary, and medical product registrations and liaising with regulatory authorities to obtain approvals.
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Medical Monitor / Medical Vigilance Officer / Medical Safety Officer
CooperCompanies
Southampton, Hampshire
8mo
Licensed UK ophthalmologist providing expert assessment of adverse events, regulatory compliance for vigilance obligations, and clinical insight into safety signals for a contact lens portfolio.
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Medical Information Specialist I (Pipeline / Fluent in English & Spanish Only)
Thermofisher
São Paulo, Brazil
9mo
Provides technical and medical information and manages intake of adverse events/product complaints for pharmaceutical and device products.
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Medication Safety Analyst
Deloitte
Imo State, ng
9mo
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.
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Medical Information Specialist I (Pipeline)
Thermofisher
São Paulo, Brazil
10mo
Provides technical and medical information and manages intake of adverse events/product complaints for pharmaceutical or device products.
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Med Info Assoc I (Pipeline)
Thermofisher
Mexico City, Mexico
10mo
Provides technical and medical information, manages intake of adverse events and product complaints, and supports clinical trial information for pharmaceutical or device products.
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Senior Consultant - Veeva Safety
Veeva
Remote
10mo
Senior consultant leading implementation of Veeva Vault Safety solutions for biopharmaceutical customers, acting as a subject matter expert in Drug Safety and Pharmacovigilance.
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(Associate) Medical Director - Neurology
Thermofisher
Remote, Portugal
11mo
Provide medical leadership and safety evaluation for clinical trials in the Pharmacovigilance department, focusing on neurology and epilepsy.
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Chile_Technical Manager
Celltrionhealthcare
Santiago, CL
12mo
Manage product registration, regulatory compliance, and pharmacovigilance for biosimilar and innovative biopharmaceutical medications in Chile.
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Consultant - Veeva Safety - Managed Services (Remote)
Veeva
Remote
1y
Drug Safety and Pharmacovigilance consultant supporting Veeva Vault Safety implementation and post-implementation managed services for biopharmaceutical customers.
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Global Head of Clinical Safety
Galderma
Barcelona
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.
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Senior Consultant - Pharmacovigilance/Safety Systems Implementation (Remote)
Veeva
Remote
$80k–$80k
1y
Lead implementations of Vault Safety solution for life sciences customers, defining business processes and guiding project delivery.
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Consultant - Vault Safety
Veeva
Remote
2y
Implement and configure Vault Safety solutions for life sciences customers, bridging the gap between existing safety systems and Veeva's platform.
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