Last updated: 2025-05-22

16 Business Development And Sales jobs in Dublin.

Hiring now: Dir Process Development @ Amgen, Associate Dir Medical Wri @ Alexion, Dir Program Ops Leader On @ Regeneron , Hcp Engagement And Contra @ Regeneron, Regulatory Affairs Consul @ Iqvia, Commercial Contracts Anal @ Inizio, Regulatory Affairs Consul @ Parexel, Medical Dir @ Medical Co.Explore more at at kaamvaam.com

🔥 Skills

Regulatory Affairs (5) project management (3) Clinical Research (3) Collaboration (3) medical writing (2) clinical study protocols (2) clinical study reports (2) Oncology (2) Clinical Trial Management (2) budget management (2)

📍 Locations

Dublin (15) Dún Laoghaire (1)

Amgen

Skills & Focus: Process Development, Drug Product Technologies, Technology Transfer, New Product Introduction, Commercial Manufacturing, Regulatory Affairs, Team Leadership, Biotechnology, GMP Compliance, Data Driven Insights
About the Company: Amgen is one of the world's preeminent biotechnology companies, reaching over 10 million patients worldwide.
Experience: 4 years in Engineering, Science or Business Management at minimum of director level
Type: Full time

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: 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…

Regeneron

Skills & Focus: HCP engagement, contracting, international markets, pharmaceutical, medical affairs, compliance, process improvements, communication, relationship management, regulatory requirements
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 growing global network to invent, de…
Experience: 3-5 years in the pharmaceutical or medical devices industry
Type: Contract
Benefits: Comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equi…

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.
Skills & Focus: Global Patient Safety, pharmacovigilance, safety strategy, clinical development, Oncology, safety documents, risk management, FDA guidelines, signal management, safety monitoring
About the Company: Regeneron is an industry-leading scientific organization working on drug development, operations, and commercialization.
Experience: Minimum 10+ years of total relevant experience in pharmacovigilance and/or relevant medical field.
Salary: $202,000.00 - $336,600.00
Type: Contract
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.

Inizio

Skills & Focus: contracts, business partnering, contract management, relationship management, negotiation, client contracts, life sciences, pharmaceutical, risk management, contract lifecycle
About the Company: A global business providing advisory, medical, marketing, and engagement services in the health and life sciences sectors, with a focus on clinical development…
Experience: Minimum of a bachelor's level degree; experience in commercial affairs / contracting role; background in Life Sciences / Pharmaceutical industry is preferable
Type: Full-time / permanent
Benefits: Package includes base salary, company bonus, pension, healthcare allowance, life assurance, 25 days annual leave, flexi…

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.

Iqvia

Skills & Focus: Customer Champion, Growth Plans, Collaboration, Promotional Activities, Targets, Retail Pharmacy Chains, Joint business plans, Healthcare, OTC medicinal brands, Dynamic Culture
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: Experience National Account Management, preferably in a fast-paced, dynamic environment.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

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