Last updated: 2025-05-22

14 Biopharmaceutical Leadership jobs in Dublin.

Hiring now: Associate Dir Medical Wri @ Alexion, Sr Mgr Clinical Study Lea @ Regeneron , Csr Appendices Oversight @ Novartis, Regulatory Affairs Consul @ Iqvia, Regulatory Affairs Consul @ Parexel, Medical Dir @ Medical Co.Explore more at at kaamvaam.com

šŸ”„ Skills

project management (4) Regulatory Affairs (4) budget management (3) Clinical Research (3) Collaboration (3) medical writing (2) clinical documents (2) regulatory submissions (2) clinical study protocols (2) clinical study reports (2)

šŸ“ Locations

Dublin (14)

Alexion

Skills & Focus: medical writing, clinical documents, regulatory submissions, clinical study protocols, clinical study reports, investigator's brochures, project management, global regulatory requirements, ICH/GCP guidelines, team player
Experience: Clinical regulatory MW experience, including global clinical studies and regulatory submissions.

Regeneron Pharmaceuticals Inc.

Skills & Focus: clinical trials, study design, regulatory compliance, project management, cross-functional team, budget management, clinical research, vendor management, protocol development, process improvement
About the Company: At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, d…
Experience: 6 years of relevant industry experience
Type: Hybrid
Benefits: Comprehensive benefits including health and wellness programs, fitness centers, equity awards, annual bonuses, and paid…
Skills & Focus: Oncology, Clinical Trial Management, Leadership, Clinical Research, Budget Management, Operational Insight, Risk Mitigation, Clinical Programs, Vendor Management, Team Management
Experience: Minimum of 12 years relevant industry experience, 8 years within clinical trial management.
Salary: $202,000.00 - $336,600.00
Type: Hybrid
Benefits: Health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off.
Skills & Focus: Clinical Trial Management, program strategy, budget management, team leadership, clinical operations, feasibility, protocol design, regulatory compliance, project management, analytical skills
About the Company: Regeneron is a biotechnology company that invents medicines for serious diseases.
Experience: 12 years in pharmaceutical industry, 8 years in Clinical Trial Management
Salary: $198,000.00 - $330,000.00
Type: Contract
Benefits: Comprehensive benefits including health and wellness programs, fitness centers, equity awards, annual bonuses, and paid…

Novartis

Skills & Focus: CSR appendices, regulatory submissions, clinical documents, vendor oversight, submission readiness, cross-functional collaboration, audit support, process improvement, clinical document management, timely submissions
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Experience: Relevant industry experience
Type: Hybrid

Alexion

Skills & Focus: medical writing, clinical regulatory documents, clinical study protocols, clinical study reports, Investigator's Brochures, regulatory requirements, ICH guidelines, oral communication, collaboration, excellent presentation skills
About the Company: Alexion's mission is to transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful v…
Experience: 3-5 years of regulatory writing experience; will consider fewer years of writing experience combined with other relevant experience.

Regeneron Pharmaceuticals Inc.

Skills & Focus: clinical trial management, leadership, strategic management, clinical operations, quality, timelines, budgets, risk mitigation, vendor management, staff recruitment
About the Company: A fully integrated biopharmaceutical company that invents life-transforming medicines for people with serious diseases.
Experience: Minimum of 12 years relevant sponsor side pharmaceutical industry experience, 8 years within clinical trial management.
Salary: $198,000.00 - $330,000.00
Type: On-site/Hybrid
Benefits: Comprehensive benefits, health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off.

Iqvia

Skills & Focus: Regulatory Affairs, pharmaceutical industry, dossiers, registration standards, dossier acquisitions, license applications, site transfers, technical variations, regulatory authorities, collaborate with CMOs
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: At least 5 years of relevant regulatory experience in the pharmaceutical industry.
Type: Part time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novartis

Skills & Focus: Quality Standards, External Service Providers, Clinical Trials, Quality Assurance, Risk Assessments, Technology Evaluation, Regulatory Compliance, Digital Health, Third-Party Management, Collaboration
About the Company: Novartis is an innovative medicines company dedicated to reimagining medicine to improve and extend people's lives with medicines that reach more than 250 mill…

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.

Medical Communications Agency

Skills & Focus: Medical Strategy, Promotional Materials, KOL Engagements, Clinical Data, Literature Searches, Medical Content, Advisory Boards, Regulatory Approval, Competitive Analyses, Client Collaboration
About the Company: A leading agency focused on delivering innovative and strategic medical communications solutions.
Experience: 10+ years in medical communications
Salary: €120,000 - €150,000
Type: Full-time
Benefits: Health insurance, retirement plan, continuing education allowance

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
Skills & Focus: Contracts, Manager, Admin, Healthcare, Biopharmaceutical, Clinical Research, Teams, Collaboration, Regulatory, Support
About the Company: Parexel is a global biopharmaceutical services organization that provides comprehensive and innovative services across the clinical development lifecycle.
Type: Full-time
Skills & Focus: Biometrics, Global Delivery, Clinical Research, Data Management, Statistical Programmers, Project Leadership, Regulatory Affairs, Clinical Trials, Machine Learning, Research Operations
About the Company: Parexel is a global biopharmaceutical services organization focused on providing innovative solutions to clients in the biopharmaceutical industry.
Type: Full-time