Last updated: 2025-05-22

12 Biopharmaceutical Leadership jobs in Prague.

Hiring now: Cell Therapy Account Lead @ Johnson Jo, Medical Monitor @ Psicro, Pv Officer @ Primevigil, Regulatory And Pv Mgr @ Ergomed, Qualified Person For Phar @ Client, Regulatory Affairs Consul @ Parexel.Explore more at at kaamvaam.com

🔥 Skills

training (4) pharmacovigilance (3) project management (3) regulatory (2) leadership (2) compliance (2) Compliance (2) Pharmacovigilance (2) clinical trials (2) Regulatory Affairs (2)

📍 Locations

Prague (12)

Johnson & Johnson

Skills & Focus: Cell Therapy, Account Management, Oncology, Hospital Operations, Site Certification, Reimbursement, Supply Chain, Stakeholder Relationships, Operational Optimization, Project Management
About the Company: Johnson & Johnson is a global healthcare company committed to improving health for humanity through innovative medicine and medical technology.
Experience: at least 5 years in key account management in a healthcare environment
Type: Full-time

Psicro

Skills & Focus: medical monitoring, clinical studies, patient safety, medical review, clinical data, SAE reports, safety monitoring, clinical documents, risk assessment, training

Primevigilance

Skills & Focus: case processing, pharmacovigilance, Individual Case Safety Reports, SAE/SUSAR Management, database outputs, PBRER, DSUR, PADER, mentoring, training
About the Company: At PrimeVigilance, PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accounta…
Experience: Demonstrated experience in case processing.

Johnson & Johnson

Skills & Focus: Medical Science Liaison, Immunology, Medical Strategy, KOLs, Educational Meetings, Market Access, Cross-functional Collaboration, Scientific Support, Patient-Centric, Healthcare Innovation
About the Company: A multinational corporation specializing in healthcare, pharmaceuticals, and medical devices.
Experience: 2-3 years in MSL/RnD or similar, expertise in Immunology preferred
Type: Full-time

Ergomed

Skills & Focus: regulatory, pharmacovigilance, leadership, project management, compliance, training, vendor management, audit readiness, regulatory intelligence, client interaction
Skills & Focus: Medical Writer, PSURs, PBRERs, PADERs, ACOs, DSURs, RMPs, Quality, Compliance, Aggregate Reports

Client

Skills & Focus: Pharmacovigilance, ICSRs, SAE, medical assessment, safety issues, Risk Management Plans, regulatory authority, signal detection, benefit-risk assessment, categorization of signals

Ergomed

Skills & Focus: pharmacovigilance, regulatory, quality, expert advice, training, audits, consultancy, regulatory documents, leadership, communication skills

Johnson & Johnson

Skills & Focus: clinical trials, healthcare innovation, clinical research, project management, regulatory compliance, GCP, team leadership, quality oversight, feasibility, site selection
About the Company: A global healthcare company dedicated to improving health and well-being through innovative medical solutions.
Experience: Minimum of 5 years in clinical research
Type: Full-time

Parexel

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.

Primevigilance

Skills & Focus: ICSR Management, Pharmacovigilance, Safety Reports, Compliance, Quality Assurance, Data Reporting, Clinical Trials, Medical Information, Reconciliation, Customer Cooperation
About the Company: PrimeVigilance is a leading provider of pharmacovigilance and regulatory services.
Type: Full-time

Parexel

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