Competitive Salary (£) | UK or US based
Boyds is looking for experienced, enthusiastic and motivated regulatory and medical writers to join our medical writing team. Working as part of the medical writing team, the successful candidates will be supporting the Boyds’ regulatory affairs, clinical operations and medical affairs teams across a range of projects, and directly with clients for standalone medical writing projects.
Role responsibilities:
- Preparation of clinical documents such as clinical study protocols and amendments, clinical study reports, and investigator’s brochures/investigator’s brochure updates
- Preparation of EU and US regulatory documents
- Project management
- Managing the document review process
- Organizing the quality control (QC) review of documents and addressing QC comments
- Editorial support and formatting of documents authored by other members of the Boyds’ teams as required
- Peer review of documents authored by other members within Boyds
- Providing guidance and training to less experienced medical writers and members of the wider Boyds team
The successful candidate will have the following qualifications and experience:
- Proven experience gained in a consultancy environment, with a minimum of a B.Sc. in a life sciences subject (a higher degree would be a distinct advantage), ideally with around 3-5 years of relevant experience or equivalent expertise would be desirable
- Excellent written and verbal communication skills, including the ability to articulate ideas clearly, engage with diverse audiences, and produce error-free written content
- Proficient in Microsoft Office with excellent skills in Word
- Experience in preparing clinical documents
- Significant experience with the preparation of EU and US regulatory documents would be a distinct advantage
- Project management skills, including the creation and maintenance of project timelines and liaison with clients
- Proven excellent time-management skills
Benefits of joining Boyds
We offer an opportunity to work with a team with significant experience in developing groundbreaking ATMP, biological and small molecule therapies for a range of conditions, many of which are rare diseases. We are a growing global drug development consultancy with a friendly, efficient and effective team and can help you to develop in a professional and varied environment. Upon successful completion of the probation period, Boyds team members are eligible for a range of attractive benefits including bonus, private healthcare, pension and the option to join the Share Incentive Scheme.
About Boyds
Boyds is a fast-growing global drug development consultancy providing a range of expertise and skills central to the development of pharmaceutical and biotechnology medicinal products and medical devices. Based in the UK, EU and US with offices in Cheshire, Cambridgeshire, Dublin and Pennsylvania, Boyds has an international client base comprising of early-stage life science and medical device companies, pharma companies and academic groups.
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If you are interested in this exciting opportunity, please state the role you are applying for in the email subject line, and send your CV and a cover letter to recruitment@boydconsultants.com
No agencies please.
