Regulatory Document Writer
2 weeks ago
Life Science Recruitment is seeking a Regulatory Document Writer to join their team.
Job Responsibilities:The successful candidate will plan, write, edit, review, and coordinate the publication of scientific data through peer-reviewed journals and forums or regulatory documents. They will also facilitate trial development and product registration, ensuring quality checks for accuracy and coordinating reviewer comments.
Responsibilities include adjusting document content as required, preparing final versions, and ensuring final documents and supporting quality check documentation are placed in the appropriate document management system.
- Plan, write, edit, review, and coordinate the publication of scientific data through peer-reviewed journals and forums or regulatory documents
- Facilitate trial development and product registration
- Ensure quality checks for accuracy and coordinate reviewer comments
A Bachelor's Degree is required, with a Graduate degree having a formal research component or in life sciences being preferred. Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience are essential. Experience in clinical trial process or regulatory activities is also required.
Candidates should have experience in writing regulatory or clinical trial documents, publication experience, and ability to work well independently and as part of a team. A writing exercise is required as part of the candidate evaluation process, and additional writing samples may be requested.
-
Regulatory Document Writer
2 weeks ago
Cork, Cork, Ireland eir evo talent Full timeAbout the Roleeir evo talent is currently looking for a highly skilled Regulatory Document Writer to join our team. As a Regulatory Document Writer, you will be responsible for ensuring that all clinical trial documents comply with ICH GCP, regulatory requirements, and internal SOPs.Key Responsibilities:Conduct thorough quality checks to ensure accuracy,...
-
Clinical Writer
2 weeks ago
Cork, Cork, Ireland Life Science Recruitment Full timeWe are seeking a skilled Medical Writer to join our client, a global life science company based in Cork.About the OpportunityThe successful candidate will collaborate with cross-functional teams to facilitate external scientific publications and regulatory documents. This is a contract role with flexible working arrangements.Key ResponsibilitiesPublishing...
-
Regulatory Compliance Writer
7 days ago
Cork, Cork, Ireland Oxford Global Resources Full timeRole OverviewOxford Global Resources is seeking a skilled Regulatory Compliance Writer to join their team. As a Regulatory Compliance Writer, you will be responsible for creating technical responses and documents for FDA audits. This is a great opportunity to use your expertise in regulatory compliance to make a real impact.Responsibilities:Collect and...
-
Regulatory Content Writer
4 hours ago
Cork, Cork, Ireland beBee Careers Full timeAbout the RoleWe are seeking an experienced medical writer to join our team as a Regulatory Content Writer. As a key member of our content development team, you will be responsible for authoring, reviewing, and finalizing high-quality clinical trial documents.Your primary focus will be on developing comprehensive study protocols, initial investigator's...
-
Cork, Cork, Ireland Pm Group Full timeThe Ideal CandidateWe are looking for a highly skilled Technical Writer/Operations Documentation Specialist with a strong background in technical writing and regulatory compliance. The ideal candidate will have a bachelor's degree in Life Sciences, Pharmaceutical Sciences, Engineering, or a related field, and at least 3-5 years of experience in technical...
-
Senior Writer for Regulatory Affairs
2 weeks ago
Cork, Cork, Ireland Oxford Global Resources Full timeAbout the Opportunity: We are seeking an experienced Senior Writer to join our team at Oxford Global Resources. As a key member of our project, you will be responsible for developing high-quality technical documents and responses that meet the strict requirements of regulatory authorities.Key Responsibilities:Develop comprehensive technical documents and...
-
Cork, Cork, Ireland Pm Group Full timeOverviewThe Outsourced Technical Services (OTS) Department at PM Group partners with Global leaders across a range of industries to find the best people for their current and ongoing business needs.Partnering with PM Group and our clients means that you will gain unrivalled experience working with global brands.We are looking for a Technical...
-
Regulatory Scientific Writer
6 days ago
Cork, Cork, Ireland Life Science Recruitment Full timeJob OverviewThe successful candidate will have a strong background in medical writing and excellent communication skills. As a Medical Writer at Life Science Recruitment, you will be responsible for creating high-quality scientific content for various regulatory and clinical trial documents. Your ability to collaborate with cross-functional teams will ensure...
-
Regulatory Document Writer
2 weeks ago
Cork, Cork, Ireland Life Science Recruitment Full timeScientific Publication CoordinatorWe are seeking a Scientific Publication Coordinator to join our team at Life Science Recruitment. The role involves collaborating with cross-functional teams to create external scientific publications and regulatory documents.About the Team:Our team is composed of experienced professionals who share a passion for science and...
-
Regulatory Document Specialist
2 weeks ago
Cork, Cork, Ireland eir evo talent Full timeJob TitleClinical Research WriterAbout the Jobeir evo talent seeks a talented Clinical Research Writer to develop high-quality clinical trial documents. The ideal candidate will have strong experience in medical writing within the clinical research industry, with a focus on Phase 1 and Phase 2 clinical trials.Key ResponsibilitiesDevelop and Review...
-
Regulatory Documentation Expert
6 days ago
Cork, Cork, Ireland Oxford Global Resources Full timeJob Summary:Oxford Global Resources seeks a seasoned Regulatory Documentation Expert to work on a project involving the creation of technical responses and documents following an FDA audit. The successful candidate will possess a strong background in regulatory documentation and experience working with pharmaceutical companies.Responsibilities:Analyze data...
-
Cork, Cork, Ireland PM Group Full timeOverviewThe Outsourced Technical Services (OTS) Department at PM Group partners with Global leaders across a range of industries to find the best people for their current and ongoing business needs. Partnering with PM Group and our clients means that you will gain unrivalled experience working with global brands.We are looking for a Technical...
-
Regulatory Compliance Writer
2 weeks ago
Cork, Cork, Ireland TN Ireland Full timeAbout You:We're looking for a skilled Medical Writer to join our team at TN Ireland. As a key member of our clinical documentation team, you will be responsible for developing high-quality clinical trial documents that support the development of innovative therapies.Requirements:Bachelor's degree in Life Sciences, Pharmacy, Medicine, or a related...
-
Regulatory Document Specialist
2 weeks ago
Cork, Cork, Ireland Life Science Recruitment Full timeLifescience Recruitment is seeking a skilled Medical Writer to join their client, a global pharma company based in Cork.Job OverviewThe successful candidate will work with cross-functional teams to facilitate external scientific publications and regulatory documents. This is a contract role with hybrid working arrangements.Key ResponsibilitiesPublishing...
-
Content Writer
3 days ago
Cork, Cork, Ireland Oxford Global Resources Full timeJob Description:OverviewOxford Global Resources seeks a seasoned Technical Writer to join our team. This eight-week project requires expertise in creating comprehensive technical documents and responses tailored to the FDA's specific requirements.ResponsibilitiesCollaborate with cross-functional teams to gather and analyze data related to post-audit...
-
Medical Writer Specialist
2 days ago
Cork, Cork, Ireland beBee Careers Full timeJob Description:">We are seeking a highly skilled Medical Writer to join our team. As a Medical Writer, you will be responsible for developing high-quality clinical trial documents, including study protocols, investigator's brochures, and clinical study reports.">Key Responsibilities:">Author, review, and finalise clinical trial documents to the highest...
-
Medical Writer
3 weeks ago
Cork, Cork, Ireland Life Science Recruitment Full timeMedical WriterOur client, a global pharma company based in Cork, is currently recruiting for a Medical Writer to join their team. As a medical writer, you will work with cross-functional, multidisciplinary teams to facilitate external scientific publications such as abstracts, posters, manuscripts, and presentations, as well as regulatory documents such as...
-
Medical Writer
1 week ago
Cork, Cork, Ireland Life Science Recruitment Full timeMedical WriterOur client, a global pharma company based in Cork, is currently recruiting for a Medical Writer to join their team. As a medical writer, you will work with cross-functional, multidisciplinary teams to facilitate external scientific publications such as abstracts, posters, manuscripts, and presentations, as well as regulatory documents such as...
-
Medical Writer
6 days ago
Cork, Cork, Ireland Life Science Recruitment Full timeOur client, a global pharma company based in Cork, is currently recruiting for a Medical Writer to join their team. As a medical writer, you will work with cross-functional, multidisciplinary teams to facilitate external scientific publications such as abstracts, posters, manuscripts, and presentations, as well as regulatory documents such as protocols,...
-
Medical Writer
2 weeks ago
Cork, Cork, Ireland Life Science Recruitment Full timeMedical WriterOur client, a global pharma company based in Cork, is currently recruiting for a Medical Writer to join their team.As a medical writer, you will work with cross-functional, multidisciplinary teams to facilitate external scientific publications such as abstracts, posters, manuscripts, and presentations, as well as regulatory documents such as...
