15 Biopharmaceutical Leadership jobs in Zagreb.

Hiring now: Clinical Research Advocat @ Milestone , Regulatory Affairs Mgr Cm @ Parexel, Pv Associate @ Primevigil, Sr Pharmacovigilance Pv P @ Ergomed, Team Lead Research @ Veeva Syst, Sr Site Activation Coordi @ Iqvia.Explore more at jobswithgpt.com.

šŸ”„ Skills

clinical trials (5) collaboration (5) clinical research (4) hospital administrators (4) Principal Investigators (4) contract negotiations (4) Regulatory Affairs (4) CMC (3) healthcare professionals (3) service provider (2)

šŸ“ Locations

Zagreb (15)

Milestone One

Skills & Focus: clinical research, HCPs, clinical trials, service provider, MDs, pharmacists, hospital administrators, Principal Investigators, contract negotiations, collaboration
About the Company: Milestone One is a leading service provider for clinical trial support and related services.

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: pharmacovigilance, drug safety, case safety reports, data entry, quality review, submissions workflow, clinical trials, reconciliation activities, supervision, mentoring
About the Company: PrimeVigilance specializes in drug safety and pharmacovigilance activities.

Ergomed

Skills & Focus: pharmacovigilance, ICSRs, signal detection, risk management, regulatory authority, adverse event, safety reports, medical review, mentoring, training

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.

Veeva Systems

Skills & Focus: leadership, operations, data production processes, compliance, quality standards, clinical trials, research team, efficiency, methodical, multi-cultural teams
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: Experience in leadership roles, preferably within the tech or life sciences sectors.
Type: Full-time
Benefits: Work Anywhere policy that supports flexibility to work from home or in the office.

Parexel

Skills & Focus: Regulatory Affairs, Consulting, Compliance, Biopharmaceutical, Clinical Trials, Regulatory Submissions, Life Sciences, Cross-functional Teams, Project Success, Global Health Authority
About the Company: Parexel is a leading Clinical Research Organization that provides comprehensive services across all phases of clinical trials, regulatory consulting, and marke…
Experience: Previous experience in regulatory affairs (level-dependent)
Benefits: Flexible work arrangements, potential for career growth, exposure to cutting-edge projects

Milestone One

Skills & Focus: clinical research, healthcare professionals, clinical trials, service provider, neurologists, hospital administrators, Principal Investigators, contract negotiations, collaboration, relationship management
About the Company: A leading service provider for clinical trial support and related services.
Experience: Experience in clinical research and relationship management
Type: Full-time

Primevigilance

Skills & Focus: Pharmacovigilance, Individual Case Safety Reports, Compliance, Data entry, Quality review, Submissions workflow, Post-marketing, Clinical trials, Triage, Reconciliation activities
About the Company: PrimeVigilance provides pharmacovigilance services, supporting contracted pharmacovigilance activities for clinical trial and post-marketing teams.

Parexel

Skills & Focus: Regulatory Affairs, CMC, Biologics, Pharmaceuticals, Submission Strategies, Quality Control, Risk Management, Project Management, Technical Documentation, Collaboration
About the Company: Parexel is a global biopharmaceutical services company that helps clients navigate the complex and ever-changing regulatory landscape.
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote/Office-based

Milestone One

Skills & Focus: clinical research, healthcare professionals, clinical trial support, onboarding oncologists, relationship building, Principal Investigators, contract negotiations, medical institutions, collaboration, hospital administrators
About the Company: Leading service provider for clinical trial support and related services.
Skills & Focus: clinical research, healthcare professionals, trials, gastroenterologists, pharmacists, hospital administrators, Principal Investigators, contract negotiations, collaboration, clinical trial support
About the Company: A service provider for clinical trial support and related services in the healthcare sector.
Experience: Experience in clinical research and relationship management preferred.
Type: Full-time

Iqvia

Skills & Focus: site activation, clinical trials, healthcare, communication, project management, regulations, SOPs, feasibility, collaboration, documentation
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: Minimum 2 years’ work experience; 1+ years in healthcare or similar
Type: Full-time

Ergomed

EU QPPV Zagreb
Skills & Focus: adverse reactions, risk evaluation, medicinal product, safety studies, oversight, available to CAs, safety profiles, emerging safety concerns, marketing authorisations, post-authorisation
Skills & Focus: medical review, lCSRs, literature review, signal detection, aggregate reports, Serious Adverse Events, periodic safety update reports, development safety update reports, database outputs, coding