28 Biopharmaceutical Leadership jobs in Dublin.

Hiring now: Regulatory Affairs Mgr Cm @ Parexel, Sr Mgr Clinical Study Lea @ Regeneron , Associate Dir Medical Wri @ Alexion, Mgr Oncology Regulatory M @ Johnson Jo, Csr Appendices Oversight @ Novartis, Sr Spec Patient Safety @ Astrazenec, Sr Mgr Clinical Study Lea @ Regeneron, Regulatory Affairs Consul @ Iqvia, Sr Mgr Clinical Study Lea @ Regeneron , Associate Dir Drug Substa @ Biomarin.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (7) project management (6) study design (5) budget management (5) vendor management (5) Regulatory Affairs (4) protocol development (4) process improvement (4) Project Management (4) data quality (4)

đź“Ť Locations

Dublin (28)
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Parexel

Regulatory Affairs Manager - CMC Biologics Dublin
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

Regeneron Pharmaceuticals Inc.

Senior Manager Clinical Study Lead (Hematology) Dublin
Skills & Focus: clinical trials, study design, project management, regulatory guidelines, budget management, cross-functional leadership, data management, risk assessment, site evaluation, clinical study delivery
About the Company: Regeneron is an equal opportunity employer and has an inclusive and diverse culture that provides comprehensive benefits.
Experience: minimum of 8 years of relevant industry experience
Salary: $148,300.00 - $241,900.00
Type: Full-time
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

Alexion

Associate Director, Medical Writing Dublin
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.

Senior Manager Clinical Study Lead Dublin
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…
Director, Program Operations Leader - Oncology Dublin
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.

Johnson & Johnson

Manager, Oncology Regulatory Medical Writing Dublin
Skills & Focus: Oncology, Regulatory Medical Writing, Clinical Documents, Project Management, People Management, Cross-functional Team, Process Improvements, Medical Writing, Scientific Strategy, 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: At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience is required.
Type: Fully Remote

Novartis

CSR Appendices Oversight Manager Dublin
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

Astrazeneca

Senior Specialist, Patient Safety Dublin
Skills & Focus: Pharmacovigilance, Patient Safety, health authority regulations, internal audits, external health authority inspections, Argus, Veeva Vault, vendor management, data analytics, cross-functional collaboration
About the Company: AstraZeneca is a science-led, global biopharmaceutical company, committed to improving the health and lives of people across the globe through our research and…
Experience: Understanding of local UK, Ireland and Malta health authority regulations. Experience in internal audits / external health authority inspections. Experience in using Pharmacovigilance systems such as Argus and Veeva Vault modules.

Novartis

Central Monitor Dublin
Skills & Focus: clinical trials, monitoring, data quality, risk management, data analytics, regulatory compliance, Good Clinical Practice, collaboration, risk identification, improvement
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…

Parexel

Various Positions Available Dublin
Skills & Focus: biostatistics, clinical trials, regulatory affairs, project leadership, statistical programming, medical writing, drug development, patient inclusion, emerging talent, clinical operations
About the Company: Parexel is a globally recognized provider of biopharmaceutical services, conducting clinical trials and providing regulatory consultancy across various therape…
Type: Remote, Full-time, Part-time, Internship
Benefits: Flexible working options, supportive atmosphere, constant learning opportunities.

Regeneron Pharmaceuticals Inc.

Senior Manager Clinical Study Lead Dublin
Skills & Focus: clinical trials, study design, budget management, protocol development, project management, data quality, clinical operations, vendor management, risk assessment, team leadership
About the Company: Regeneron is an innovative biopharmaceutical company that invents life-transforming medicines for people with serious diseases.
Experience: minimum of 8 years of relevant industry experience
Salary: $148,300.00 - $241,900.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees

Regeneron

Senior Manager, Clinical Study Lead (hematology) Dublin
Skills & Focus: clinical trials, project management, study design, budget management, stakeholder engagement, risk mitigation, data quality, clinical operations, protocol development, vendor management
Experience: Minimum of 8 years of relevant industry experience.
Salary: $145,400.00 - $237,200.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off.

Parexel

Regulatory Affairs Manager - CMC biologics Dublin
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.

Iqvia

Regulatory Affairs Consultant Dublin
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

Global Regulatory Publishing Associate Dublin
Skills & Focus: regulatory, publishing, clinical deliverables, global submissions, quality reviews, validation, archiving, collaboration, electronic document, continuous improvement
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: Experience with electronic clinical document publishing standards/formats, electronic and global regulatory submission publishing standards/formats (e.g. eCTD, EU CTR)
Type: Hybrid

Astrazeneca

Medical Science Liaison - 6 Month Secondment/FTC Dublin
Skills & Focus: Medical Science Liaison, Complement indications, Patient outcomes, Scientific engagement, Healthcare professionals, Clinical data, Rare diseases, Medical Affairs, Pharmaceutical regulations, Project management
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies.
Experience: 3-5 years experience in Medical Affairs or the Irish healthcare environment
Salary: Competitive Salary & Benefits
Type: Contract

Parexel

Project Manager Supply & Logistics Dublin
Skills & Focus: Project Manager, Supply Chain, Logistics, Clinical Trials, Remote Work, Project Leadership, Regulatory Affairs, Data Management, Clinical Research, Vendor Management

Novartis

Global Program Associate Director Dublin
Skills & Focus: Drug Development, Project Management, Global Program Management, Project Plans, Cross-functional Teams, Risk Management, Program Strategy, Executive Communication, Operational Support, Portfolio Decisions
About the Company: Novartis is an innovative medicines company that works to improve and extend people's lives.
Type: Full-time

Regeneron Pharmaceuticals

Senior Manager Clinical Study Lead Dublin
Skills & Focus: clinical trials, study design, project management, risk assessment, clinical study, budget management, protocol development, vendor management, regulatory compliance, data quality
Experience: 8 years of relevant industry experience
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

Astrazeneca

Personal Assistant & Administration Team Lead, Precision Medicine and Biosample… Dublin
Skills & Focus: administrative support, diary management, travel coordination, performance management, team meetings, confidentiality, process improvement, logistical support, business planning, employee onboarding
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, focused on delivering life-changing medicines and fostering …
Experience: Significant personal assistant/ administrative or related experience; Experience of leading teams.
Type: Full-time
Benefits: Inclusive and diverse team culture, supportive management, life-changing work assignments.

Biomarin

Associate Director, Drug Substance Technology Transfer Dublin
Skills & Focus: Technical Operations, Drug Substance, Technology Transfer, Manufacturing, Quality Assurance, Project Execution, Team Leadership, Regulatory Compliance, Collaboration, Drug Development
About the Company: BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commer…
Experience: 10+ years of professional experience in the pharmaceutical industry, including managerial experience.
Type: Hybrid
Director, Drug Product Technology Transfer Dublin
Skills & Focus: Drug Product Technology Transfer, cGMP, Quality Systems, Project Execution, Process Development, Technical Leadership, Team Management, Regulatory Filing, Collaboration, Biopharma
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: 10+ years of professional experience in the pharmaceutical industry, including managerial experience
Type: Hybrid

Emergent Biosolutions

Director, Regulatory Affairs EU Dublin
Skills & Focus: regulatory affairs, EU regulations, biotechnology, pharmaceutical industry, licensure, strategic direction, regulatory guidance, clinical development, health authority meetings, product portfolio
About the Company: Emergent BioSolutions focuses on protecting and enhancing lives by developing products designed to protect life.
Experience: 12+ years directly related experience in Regulatory Affairs, in biotechnology or pharmaceutical industry.
Benefits: competitive salaries, flexible work arrangements and an extensive benefits package

Eversana1

Medical Director Dublin
Skills & Focus: medical strategy, medical content, promotional efforts, clinical data, literature searches, medical conferences, competitive analyses, KOL materials, advisory boards, medical/regulatory approval

Alexion

Senior Manager, Medical Writing Dublin
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.

Biomarin

Vice President, Head of Analytical Sciences Dublin
Skills & Focus: analytical sciences, pharmaceutical, leadership, drug development, biotechnology, QC laboratories, analytics, regulatory guidelines, method development, quality assurance
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: Minimum of 15 years of experience in analytical development or QC laboratories within the pharmaceutical industry.
Type: Hybrid

Astrazeneca

R&D Diagnostic Alliance and Project Manager Dublin
Skills & Focus: Diagnostic Alliance Manager, Project Management, Partnership Governance, Risk Management, Project Plans, Collaboration, Precision Medicine, Stakeholder Management, Regulatory Compliance, Contracting Process
About the Company: AstraZeneca is one of the leading pharmaceutical companies in precision medicine, transforming patients’ lives by personalizing treatment.
Experience: Significant experience within a scientific project management environment

Bausch Health

Professional Affairs Manager (EMEA) Dublin
Skills & Focus: professional programs, KOL management, medical insights, educational programs, business relationships, customer insights, project plans, process improvement, budget forecasting, clinical studies
About the Company: We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. We develop, manufacture and …
Experience: 5+ years of experience in professional, clinical and/or medical affairs within the medical device industry
Type: Full-time