Last updated: 2025-05-22

10 Biopharmaceutical Leadership jobs in Bucharest.

Hiring now: Sr Pharmacovigilance Phys @ Ergomed, Pharmacovigilance Spec @ Pharmaceut, Post Market Surveillance @ Stryker, Clinical Research Associa @ Alimentiv2, Medical Devices Adverse E @ Baxter, Medical Monitor @ Psicro, Regulatory Affairs Consul @ Parexel.Explore more at at kaamvaam.com

🔥 Skills

Regulatory Affairs (4) medical review (3) Pharmacovigilance (2) adverse events (2) Safety Reports (2) Risk Management (2) Clinical Trials (2) medical device regulations (2) Clinical Research (2) ICSRs (1)

📍 Locations

Bucharest (10)
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Ergomed

Senior Pharmacovigilance Physician I Bucharest
Skills & Focus: Pharmacovigilance, ICSRs, signal detection, risk management, QPPV, adverse events, medical review, Safety Reports, regulatory authority, mentoring

Pharmaceutical Company

Pharmacovigilance Specialist Bucharest
Skills & Focus: Pharmacovigilance, ICSR, SAE, Risk Management, Safety Reports, Clinical Trials, Benefit-Risk Assessment, Signal Detection, Regulatory Compliance, Drug Safety
About the Company: A leading company in the pharmaceutical sector focusing on drug safety and pharmacovigilance.
Experience: 3+ years in pharmacovigilance
Salary: Competitive
Type: Full-time
Benefits: Health insurance, retirement plan, paid vacation

Stryker

Post Market Surveillance Senior Specialist Bucharest
Skills & Focus: PMS activities, post market strategy, product safety issues, regulatory authorities, regulatory intelligence, compliance activities, SOPs development, continuous improvement, training materials, medical device regulations
About the Company: Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative product…
Experience: Minimum 2 years’ experience
Type: Full Time
Benefits: bonuses, healthcare, insurance benefits, retirement programs, wellness programs, service and performance awards, variou…

Alimentiv-2

Clinical Research Associate Bucharest
Skills & Focus: clinical site monitoring, training, CRA skills, protocol compliance, SOP compliance, regulatory compliance, site management, investigative site, patient recruitment, data monitoring
Type: Full-time

Baxter

Medical Devices Adverse Events Reviewer Bucharest
Skills & Focus: medical review, adverse events, safety signaling, stakeholder insight, negotiation skills, strategic planning, complaints monitoring, clinical investigation, data entry, medical device regulations
About the Company: Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, they have pioneered significant me…
Experience: At least 5 years of medical professional experience, including 2 years related clinical, safety, pharmacovigilance or regulatory experience in the medical device industry.
Benefits: Employee Health & Well-Being Benefits, Paid Time Off, Continuing Education/Professional Development, 2 Days a Year to V…

Psicro

Medical Monitor Bucharest
Skills & Focus: medical monitoring, clinical studies, patient safety, clinical development, data safety monitoring, clinical data analysis, SAE reports, medical review, clinical training, risk assessment

Parexel

Regulatory Affairs Consultant - CMC biologics Bucharest
Skills & Focus: Regulatory Affairs, CMC, Pharmaceutical, Biologics, Quality Control, Submission Strategies, Market Expansions, Risk Management, Collaboration, Technical Documentation
About the Company: Parexel is a global biopharmaceutical services company that provides expertise in regulatory affairs, clinical research, and other related fields to help bring…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, supportive and inclusive environment, opportunities for career growth.
Regulatory Affairs Project Manager Bucharest
Skills & Focus: Regulatory Affairs, project management, clinical trials, client relationships, compliance, project execution, budget management, resource planning, cross-functional teams, therapeutic areas
About the Company: Parexel is a global biopharmaceutical services organization that provides a broad range of expertise to support the development and market access of innovative…
Experience: extensive experience in Regulatory Affairs, PMP or equivalent certification preferred
Regulatory Affairs Consultant - Global Asset Lead Bucharest
Skills & Focus: Regulatory Affairs, Consulting, Clinical Research, Biopharmaceutical, Asset Lead, Home-based, Remote, Project Management, Life Sciences, Medical Writing
About the Company: Parexel is a global biopharmaceutical services organization dedicated to providing expertise and resources for clinical research.
Type: Consulting