
Scientific Writer Regulatory
6 days ago
Scientific Writer RegulatoryOur client, a global pharma company, are currently growing their Global Scientific Communications team and are currently seeking a skilled Scientific Writer Regulatory to join their team on a permanent basis. As Scientific Writer Regulatory you will be responsible for the creation of high-quality regulatory documents (e.g., clinical study reports, briefing packages, regulatory responses, IND/MAA submissions). The role involves collaborating with cross-functional teams to ensure clear, accurate, and compliant scientific content throughout the drug development lifecycle. This role offers hybrid working.
Responsibilities- Document Development: Plan, write, edit, and finalize regulatory documents; ensure data accuracy, clarity, and consistency; coordinate reviews and incorporate feedback.
- Project Management: Develop timelines, manage risks, track progress, and maintain communication with stakeholders to deliver on schedule.
- Scientific Expertise: Maintain up-to-date knowledge of assigned therapeutic areas, compounds, and relevant regulatory guidelines.
- Collaboration & Coaching: Share best practices, provide guidance to colleagues, and contribute to process improvements.
- Bachelor's degree in life sciences, health, communications, or related field.
- Advanced degree with research background.
- Expertise in relevant therapeutic areas (e.g., oncology, neuroscience, immunology).
- Experience with clinical development and regulatory submissions.
- Proven experience in regulatory or technical scientific writing.
- Strong communication, interpersonal, and project management skills.
- Proficiency with document management systems and standard software tools.
-
Scientific Writer Regulatory
3 weeks ago
Cork, Cork, Ireland Life Science Recruitment Ltd Full timeScientific Writer Regulatory Our client, a global pharma company, are currently growing their Global Scientific Communications team and are currently seeking a skilled Scientific Writer Regulatory to join their team on a permanent basis.As Scientific Writer Regulatory you will be responsible for the creation of high-quality regulatory documents (e.g.,...
-
Regulatory Scientific Writer
5 days ago
Cork, Cork, Ireland beBeeRegulatory Full time €50,000 - €80,000Job Title: Regulatory Scientific WriterAre you a skilled scientific writer looking for a new challenge? Our client is seeking a talented Regulatory Scientific Writer to join their Global Scientific Communications team.This role involves creating high-quality regulatory documents, including clinical study reports, briefing packages, and regulatory responses....
-
Scientific Writer Publications
5 days ago
Cork, Cork, Ireland Scientificjobs Full timeScientific WriterPublications Our client, a global pharmaceutical organisation are currently recruiting for a Scientific WriterPublications to join their growing Global Scientific Communications team. As Scientific Writer Publications, you will work with cross-functional, multidisciplinary teams to prepare scientific publications including abstracts,...
-
Scientific Content Developer
5 days ago
Cork, Cork, Ireland beBeePublications Full time €65,000 - €85,000Scientific Writer - Publications SpecialistOur client, a global pharmaceutical organization, are currently recruiting for a Scientific Writer - Publications Specialist to join their growing Global Communications team. As a key member of the team, you will work with cross-functional, multidisciplinary teams to prepare scientific publications, including...
-
Regulatory Content Specialist
5 days ago
Cork, Cork, Ireland beBeeRegulatory Full time €83,000 - €97,000Job Opportunity: Scientific Writer Regulatory\Our organization seeks a skilled Scientific Writer Regulatory to join our team. As Scientific Writer Regulatory, you will be responsible for creating high-quality regulatory documents.\Key Responsibilities:\\Develop and finalize regulatory documents, ensuring data accuracy, clarity, and consistency.\Collaborate...
-
Senior Scientific Content Developer
6 days ago
Cork, Cork, Ireland beBeeBiotech Full time €60,000 - €80,000Scientific Writer - PublicationsThis role requires a skilled writer to prepare scientific publications, including abstracts, posters, manuscripts, presentations, and regulatory documents.Key responsibilities include document preparation, development, and finalization/document management.Evaluate data, information, and input from multiple sources, functions,...
-
Scientific Publications Specialist
7 days ago
Cork, Cork, Ireland beBeeScientific Full time €60,000 - €80,000Are you a skilled writer and communicator looking for a challenging opportunity to showcase your expertise? As a Scientific Publications Specialist, you will play a critical role in preparing high-quality scientific publications and regulatory documents that effectively communicate complex information to various audiences.Key Responsibilities:Prepare and...
-
Technical Writer
7 days ago
Cork, Cork, Ireland Quanta Consultancy Services Ltd Full timeTechnical Writer - Ireland, Cork - 12 Month ContractAre you interested in joining a world-leading biopharmaceutical company focused on developing advanced and innovative treatments for those suffering from rare diseases?This is a fantastic opportunity to work in a state-of-the-art facility in Cork.You will be joining a leading biopharmaceutical company that...
-
Technical Writer
7 days ago
Cork, Cork, Ireland Qcs Staffing Ltd Full time2 days ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Technical Writer - Ireland, Cork - 12 Month ContractAre you interested in joining a world-leading biopharmaceutical company focused on developing advanced and innovative treatments for those suffering from rare diseases?This is a fantastic opportunity to...
-
Senior Regulatory Document Specialist
5 days ago
Cork, Cork, Ireland beBeeRegulatory Full time €55,000 - €85,000Job DescriptionWe are seeking a skilled Regulatory Writer to join our team on a permanent basis. The role involves creating high-quality regulatory documents such as clinical study reports, briefing packages, and IND/MAA submissions.Main ResponsibilitiesDevelop comprehensive regulatory documents ensuring data accuracy and compliance with relevant...