Author Jobs in Bedfordshire
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Search results - Author Jobs in Bedfordshire
Sonovision UK - Ortec GroupLuton
Sonovision UK is a leading provider of Engineering Support Services to clients. Our experts help our clients in the Energy, Aerospace, Military and Commercial Sectors achieve time-to-market objectives and cost goals.
The Technical Author...
RandstadBedford
development teams to support new product development and change control, ensuring compliance with US, EU, and other global regulatory requirements.
• Author EU technical documentation under MDR, FDA submissions (e.g., 510(k)) and other global regulatory...
Planet PharmaBedford
including vendor management
• Apply good publication practices and ensure compliance with global SOPs and documentation requirements
• Review publication drafts for scientific quality and alignment with author direction
• Track budgets, report on progress...
Love SuccessBedford
ethics.
Responsibilities:
• Accurate assessment of activities by authors, reviewers, editors, guest editors and others
• Assessing large-scale investigations including plagiarism, duplication, authorship disputes, peer review manipulation, and figure...
Planet PharmaLuton
including vendor management
• Apply good publication practices and ensure compliance with global SOPs and documentation requirements
• Review publication drafts for scientific quality and alignment with author direction
• Track budgets, report on progress...
The RFT GroupBedford
intelligence to internal stakeholders and assist in preparing the organization for any internal adaptation that may be required.
Author, review, and update RA SOPs as needed, with emphasis on clinical regulatory processes.
Maintain links with external...
The RFT GroupBedford
Medical Affairs, etc.
The successful candidate will author, review and manage clinical documents, e.g., clinical study protocols and/or amendments, investigator brochures, clinical study reports and clinical summaries, and regulatory development documents...
Catch Resource ManagementLuton
end users and to product suppliers/authors.
Our consultants deliver a completely professional resourcing service, always backed up by our team of ERP specialists who are all experienced in full project life cycle implementation and support, thus...
The RFT GroupLuton
Medical Affairs, etc.
The successful candidate will author, review and manage clinical documents, e.g., clinical study protocols and/or amendments, investigator brochures, clinical study reports and clinical summaries, and regulatory development documents...
Environment AgencyEngland
Job Description
Do you want to make a lasting positive change to the environment? As a Technical author in the UK BAT team you can.
We are fully committed to having an inclusive workforce to reflect the communities we serve. We welcome flexible...
Fengkai Group Co., LimitedEngland
Job Opening: Proofreading Editor for Social Sciences, Education, and Management
About Us:
We are Fengkai Group, a leading academic service provider committed to offering high-quality academic support to researchers and authors. We help authors...
Planet PharmaBedford
and interpret statistical outputs, author statistical sections of clinical study reports (CSRs), and contribute to publications and presentations.
• Stay abreast of methodological advances in oncology statistics and apply innovative approaches where appropriate...
Planet PharmaEngland
including vendor management
• Apply good publication practices and ensure compliance with global SOPs and documentation requirements
• Review publication drafts for scientific quality and alignment with author direction
• Track budgets, report on progress...
1 similar job: Newport
Planet PharmaLuton
and interpret statistical outputs, author statistical sections of clinical study reports (CSRs), and contribute to publications and presentations.
• Stay abreast of methodological advances in oncology statistics and apply innovative approaches where appropriate...
The RFT GroupLuton
Operations, Regulatory Affairs, Medical Affairs, Commercial, etc.
The successful candidate will author, review and manage clinical documents, e.g., clinical study protocols and/or amendments, investigator brochures, clinical study reports and clinical...
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