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Healthcare
› Pharmacovigilance
Pharmacovigilance
362 open positions
Drug Safety Physician
Ire
Ciudad de México, México
1mo
Provide medical and safety support to clinical research projects, ensuring adherence to ethical principles, GCP, and pharmacovigilance standards.
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Remote - Medical Information Associate (Fresher - B.Pharm/PharmD/Nursing)
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Apcer Life Sciences
Remote
$65k–$65k
1mo
Responds to medical inquiries and complaints from physicians, pharmacies, and consumers; manages adverse event reporting and maintains accurate product information.
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PATIENT SAFETY SENIOR MANAGER
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Almirall
Sant Feliu de Llobregat, CT, ES
1mo
Manage corporate pharmacovigilance activities to ensure patient safety for marketed and investigational products.
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Associate Director, Drug Safety Physician, Medical Review
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Takeda Pharmaceuticals
KA, IN
1mo
Oversee medical assessment of individual case safety reports for investigational and marketed products across all therapeutic areas to ensure regulatory compliance.
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Director, Global Patient Safety Business Office
Regeneron
TARRYTOWN, US
$183k–$183k
1mo
Strategic partner to the SVP of Global Patient Safety driving execution of the department's strategic plan, operating plans, and transformation initiatives for pharmacovigilance (PV) enablement.
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Director, Pharmacovigilance Hub
Regeneron
TARRYTOWN, US
$183k–$183k
1mo
Oversees country/regional Pharmacovigilance execution, ensuring local safety activities meet global standards and regulatory requirements while integrating data into the global PV system.
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Drug Safety Physician
ICON Clinical Research
Ciudad de México, México
1mo
Provide medical and safety support to clinical research and pharmacovigilance activities, ensuring projects meet ethical principles, GCP, and regulatory standards.
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Manager, Local Pharmacovigilance
Myhrabc
NCEE > Hungary > Remote
1mo
Manage local pharmacovigilance systems, ensuring compliance with national laws, overseeing ICSR collection, signal detection, and liaison with competent authorities.
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Senior Specialist, Local Pharmacovigilance
Myhrabc
NCEE > Greece > Remote
1mo
Manage local pharmacovigilance systems, oversee safety reporting, and ensure compliance with national laws for pharmaceutical products.
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Pharmacovigilance Analyst
Myhrabc
LATAM > Brazil > Remote
1mo
Maintain oversight of local pharmacovigilance (PV) systems to ensure compliance with national laws and regulations, manage local ICSR, conduct literature searches, and implement risk minimization measures.
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Pharmacovigilance Analyst
↗
Cencora
Brasília, DF, BR
1mo
Maintain oversight of local pharmacovigilance (PV) systems to ensure compliance with national laws and regulations, managing local literature searches, ICSR management, and risk minimization measures.
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Senior Specialist, Client Facing Scientific Consulting
Myhrabc
Remote, Lithuania
1mo
Manage local pharmacovigilance systems, oversee safety reporting, and act as the official liaison with national health authorities for a pharmaceutical client.
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Safety Scientist II/ III, EMEA
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Thermo Fisher Scientific
Remoto, PT
1mo
Manage the safety profile of new drugs in clinical trials, oversee case-processing activities, and perform regulatory reporting and medical monitoring tasks.
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Safety Scientist II/ III, EMEA
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Thermo Fisher Scientific
En remoto, ES
1mo
Manage the safety profile of new drugs in clinical trials, oversee case-processing activities, and perform regulatory reporting and medical monitoring tasks.
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Sr. Safety Specialist
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サイネオス・ヘルス
Buenos Aires, B, AR
1mo
Senior Safety & Pharmacovigilance Specialist responsible for ICSR collection, processing, reporting, literature screening, drug coding, and preparation of safety reports for clinical trials and post-marketing programs.
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Drug Safety Physician
Icon
Mexico, Mexico City
1mo
Provide medical and safety support to clinical research projects, ensuring adherence to ethical principles, GCP, and pharmacovigilance standards.
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Global Product Safety Science Lead
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Sobi - Swedish Orphan Biovitrum AB (publ)
Cambridge, England, UK
1mo
Lead safety surveillance, benefit-risk evaluation, and signal detection for assigned pharmaceutical products across the lifecycle.
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Senior Medical Director, Product Safety Physician Lead
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Beone Medicines
Remote, US
1mo
Lead Product Safety Physician overseeing benefit/risk safety profiles for multiple complex developmental programs, managing global safety data interpretation, and ensuring patient safety across the product lifecycle.
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Senior Manager
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Cencora
Madrid, MD, ES
1mo
Deliver client engagements and work products related to pharmacovigilance, safety surveillance, risk management, and scientific consulting services.
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Senior Manager
Myhrabc
Madrid, Spain
1mo
Lead pharmacovigilance and drug safety operations to ensure compliant safety deliverables, signal detection, and risk management for clients.
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Medical Director M-SERM
↗
Thermo Fisher Scientific
São Paulo, SP, BR
1mo
Lead medical safety evaluation and risk management for clinical trials and pharmacovigilance activities.
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Medical Director M-SERM
Thermofisher
Remote, Colombia, AR
1mo
Lead medical safety evaluation and risk management efforts, including reviewing adverse events, managing signal detection, and ensuring accurate medical content in regulatory reports.
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Senior Submissions Officer
Ergomed
Raleigh, NC, us
1mo
Supports clients in safety submission processes, regulatory reporting, and pharmacovigilance operations for pharmaceutical treatments.
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Medication Officer
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Nerd Nirvana
UP, IN
$216k–$336k
1mo
Oversee safe, effective, and compliant use of medicines; lead clinical risk management and track medication errors to minimize patient harm.
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Pharmacovigilance Specialist - US - Remote
↗
Worldwide Clinical Trials
Remote
$50k–$50k
1mo
Collect, process, evaluate, and report Serious Adverse Event (SAE) data for clinical trials, serving as a lead on small to moderate complexity studies.
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Sr Medical Director Risk Management, Global Pharmacovigilance
Gehc
BeiJing
1mo
Strategic leadership for global product safety risk management, benefit-risk evaluation, and safety signal governance across the product lifecycle.
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Associate Case Processing Manager (Line Management position)
Ergomed
Rome, Lazio, it
1mo
Leads the ICSR management team for specific projects, overseeing workflow, client cooperation, and staff line management within a pharmacovigilance context.
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Associate Case Processing Manager (Line Management position)
Ergomed
Prague, Prague, cz
1mo
Line manages a team responsible for Individual Case Safety Report (ICSR) management and processing for life science clients.
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Pharmacovigilance Coordinator (Japanese Skills Required)
Psi-Cro
Bangkok, Bangkok, th
1mo
Provide day-to-day support to the global Pharmacovigilance Department and In-country Clinical Caretaker by processing and reporting safety information throughout clinical trials.
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Pharmacovigilance ICSR Intern
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Medifodil Smart Pharma Solutions
TS, IN
$144k–$144k
1mo
Intern processing Individual Case Safety Reports (ICSRs) and managing adverse event data for pharmaceutical and medical device companies.
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Senior Safety & PV Ops Specialist - Technology Support (ARGUS Console or Veeva Safety preferred) - Argentina, Mexico, Brasil - Remote
↗
サイネオス・ヘルス
Remote
1mo
Senior technical support specialist for pharmacovigilance (PV) systems and safety technology platforms, ensuring system reliability, compliance, and operational continuity.
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Senior Manager, Global Patient Safety
Regeneron
Tokyo
1mo
Oversee Japan pharmacovigilance reporting, compliance, and safety operations for a global biopharma company.
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Senior Pharmacovigilance Project Manager- Europe
Ergomed
Sofia, Sofia City Province, bg
1mo
Managing pharmacovigilance projects for clients, ensuring service delivery meets expectations and aligns with signed agreements.
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Associate Pharmacovigilance Project Director (Delivery)- Europe
Ergomed
Madrid, MD, es
1mo
Deliver contracted pharmacovigilance activities for clients within budget, timeline, and regulatory compliance while managing project scope and quality.
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Assoc Dir, Pharmacovigilance
↗
Iqvia
KA, IN
1mo
Lead and manage offshore service delivery teams to support global Pharmacovigilance projects, focusing on identifying and documenting Adverse Events (AEs) and Product Quality Complaints (PQCs) for regulatory reporting.
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Senior Manager - Investigation
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Abbott
MH, IN
1mo
Conduct internal investigations into alleged violations of the Abbott Code of Business Conduct, analyze reports, interview witnesses, and recommend corrective actions.
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Medical Director
Thermofisher
Prague, Czechia
1mo
Provide medical oversight and strategic leadership for Phase I–IV clinical trials and marketed product safety, ensuring regulatory compliance and patient safety.
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Senior Pharmacovigilance Associate
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ICON Plc
TN, IN
1mo
Managing and overseeing pharmacovigilance activities to ensure the safety and efficacy of pharmaceutical products, including processing adverse event reports and analyzing safety data.
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Senior Safety Committee Specialist - Adjudication
↗
Thermo Fisher Scientific
São Paulo, SP, BR
1mo
Lead complex safety projects and ensure implementation of pharmacovigilance practices for Clinical Evaluation Committees (CEC) and Data and Safety Monitoring Boards (DSMB) to support product safety and efficacy.
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French to English for Life Sciences / Pharmacovigilance Linguist
Welo Global
Remote
1mo
Translating and reviewing high-volume safety and regulatory content (adverse event reports, clinical documentation) from French to English for a global pharmaceutical company.
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Senior Director Global Investigations & Compliance Monitoring
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Biontech
Mainz, RP, DE
1mo
Lead global internal investigations, speak-up processes, and disciplinary recommendations to safeguard BioNTech's integrity and ethical standards.
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Associate Director, Global CST, Pharmacovigilance PSMF and Business Process Management
Madrigalpharma
PA - Conshohocken - Office
$167k–$167k
1mo
Manage the Pharmacovigilance System Master File (PSMF) life-cycle and optimize global business processes for pharmacovigilance compliance.
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Associate Medical Director / Oncologist (Brazil)
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Allucent
Remote
1mo
Ensure medical/clinical and safety integrity and quality of oncology clinical trials, serving as the medical monitor contact for investigators and study sites.
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Associate Medical Director / Oncologist (USA)
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Allucent
Remote
1mo
Ensure medical/clinical and safety integrity of oncology clinical trials by serving as the medical monitor contact for investigators and study sites.
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Safety Physician TA Lead - Oncology
AstraZeneca
Shanghai Jing'An Office, CN
1mo
Lead clinical safety strategy and risk management for oncology products in China, overseeing a team and managing signal detection and regulatory compliance.
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Associate Medical Director / Neurologist (Brazil)
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Allucent
Remote
1mo
Ensure medical/clinical and safety integrity and quality of trials for small-medium biopharmaceutical companies, serving as the medical monitor contact for study protocols and safety.
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Pharmacovigilance Coordinator
Psi-Cro
Tokyo/Osaka, jp
1mo
Provide day-to-day support to the global Pharmacovigilance Department and In-country Clinical Caretaker by processing and reporting safety information throughout clinical trials.
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Senior Medical Project Coordinator
ThermoFisher Scientific
México
1mo
Manage, coordinate, and evaluate medical projects for pharmaceutical and biotechnology programs, ensuring compliance and optimal performance throughout the project lifecycle.
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Associate Medical Director, Drug Safety
↗
Biogen
Remote, US
$184k–$184k
1mo
Global pharmacovigilance for investigational and marketed products, including safety data analysis, signal identification, and benefit-risk profiling.
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Associate Medical Safety Director
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Iqvia
Remote
1mo
Provide medical expertise on pharmacovigilance services, reviewing adverse events, safety reports, and regulatory documents for clinical trials and stand-alone safety projects.
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