17 Biopharmaceutical Leadership jobs in Prague.

Hiring now: Regulatory Affairs Mgr Cm @ Parexel, Pv Officer @ Primevigil, Pharmacovigilance Analyst @ Iqvia, Medical Monitor @ Psi, Lead Local Trial Mgr @ Johnson Jo, Medical Reviewer I @ Ergomed, Medical Science Liaison O @ Astrazenec, Local Trial Mgr @ Amgen.Explore more at jobswithgpt.com.

🔥 Skills

Regulatory Affairs (3) Clinical Research (3) pharmacovigilance (3) project management (3) CMC (2) Data Management (2) Statistical Programming (2) Biostatistics (2) Individual Case Safety Reports (2) mentoring (2)

📍 Locations

Prague (17)

Parexel

Skills & Focus: Regulatory Affairs, CMC, Biologics, Project Leadership, Clinical Research, Data Management, Statistical Programming, Consulting, Medical Writing, Biostatistics
About the Company: Parexel is a global biopharmaceutical services organization that provides a range of services to enhance the clinical development of drugs and medical devices.
Type: Full-time

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.

Parexel

Skills & Focus: Regulatory Affairs, CMC, Life Sciences, Biopharmaceuticals, Quality Assurance, Submission Strategies, Technical Documentation, Project Management, Risk Mitigation, Collaboration
About the Company: Parexel is a global biopharmaceutical services organization that provides expertise and solutions to companies in the life sciences sector, helping them to nav…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, opportunities for career growth, and a supportive work environment.
Skills & Focus: Clinical Programmer, data review, trial management, SQL, programming, clinical trial, data reporting, Biotechnology, Pharmaceutical, Life Sciences
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the t…
Experience: Minimum of 5 years of experience in developing software in a clinical trial environment using SQL, including at least 3 years of clinical programming experience.

Iqvia

Skills & Focus: Pharmacovigilance, Compliance, Data Entry, Safety Cases, Market Research, Analyses, Client Management, Reporting, Safety Data, Training
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Working knowledge of pharmacovigilance requirements and processes.
Type: Contract
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Skills & Focus: Biostatistics, Statistical Programming, Data Management, Clinical Trials, Procurement, Clinical Research, Clinical Programmer, Remote Work, Global Clinical Operations, Research Organization
About the Company: Parexel is a global clinical research organization that provides comprehensive drug development services to the pharmaceutical and biotechnology industries.
Type: Remote

Psi

Skills & Focus: Medical point of contact, clinical trials, GCP guidelines, data safety monitoring, clinical development plans, clinical data review, mitigation strategies, safety monitoring boards, compliance, Pharmacovigilance
About the Company: Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and wel…

Johnson & Johnson

Skills & Focus: clinical trial management, data generation, protocol oversight, Good Clinical Practice (GCP), regulatory requirements, site selection, budget forecasting, adverse events, project planning, vendor services
About the Company: Johnson & Johnson is a global leader in the healthcare sector, committed to innovation in areas such as pharmaceuticals, medical devices, and consumer health p…
Experience: At least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience.
Type: Full-time
Skills & Focus: Therapeutic Area, Product Management, Sales Force, Commercial Plans, Market Access, Customer Engagement, Resource Allocation, Market Insights, Business Strategy, Leadership
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 3-5 years
Type: Full-time
Benefits: An opportunity to be part of a global market leader, a dynamic and inspiring working environment, opportunities for cha…
Skills & Focus: Medical Science Liaison, Immunology, Medical Affairs, Scientific support, Customer partnerships, Medical strategy, Cross-functional collaboration, Patient health, Clinical expertise, Training
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 2-3 years of previous experience in MSL/ RnD or a comparable position and expertise in Immunology preferred.
Type: Full-time

Ergomed

Skills & Focus: medical review, Individual Case Safety Reports, Serious Adverse Event, signal detection, literature review, aggregate reports, causality assessment, Periodic Safety Update Reports, Development Safety Update Reports, safety related findings

Astrazeneca

Skills & Focus: Medical Science Liaison, Oncology, healthcare professionals, medical insights, strategic programs, medical education, pharmaceutical, biotechnology, project management, customer orientation
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies dedicated to innovation in the field and focused on deliverin…
Experience: University degree (or equivalent experience) in medicine, pharmacology, natural, or health sciences, preferably in a similar MSL role.

Amgen

Skills & Focus: clinical trials, project management, study implementation, country strategy, collaboration, cross-functional teams, risk mitigation, audit support, vendor management, clinical research
About the Company: Amgen is a biotechnology company that develops and delivers innovative therapies.
Experience: Doctorate degree OR Master’s degree & 3 years of directly related experience OR Bachelor’s degree & 5 years of directly related experience OR Associate’s degree & 10 years of directly related experience OR High school diploma / GED & 12 years of directly related experience
Type: Full time

Ergomed

Skills & Focus: pharmacovigilance, regulatory, quality, expert advice, training, audits, consultancy, regulatory documents, leadership, communication skills
Skills & Focus: pharmacovigilance, medical review, ICSRs, signal detection, aggregate reports, risk management, safety reports, mentoring, qualified person, regulatory authority

Iqvia

Skills & Focus: Clinical Research, monitoring, site selection, regulatory requirements, Good Clinical Practice, project management, data integrity, collaboration, Czech, English
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Experience as a Clinical Research Associate for almost two years.
Type: Full time
Benefits: Company car, mobile phone and attractive benefits package