CK Group are recruiting for a Senior Regulatory and Medical Writer to join a leading, dynamic and fast-growing consultancy on a permanent basis. They specialise in Advanced Therapies and Rare Diseases. This will be a fully remote role and candidates looking for permanent, contract or part-time roles will be considered.
RESPONSIBILITIES:
Working as part of the medical writing team, you will be supporting the regulatory affairs, clinical operations and medical affairs teams across a range of projects, and directly with clients for standalone medical writing projects.
* 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 team members as required.
* Peer review of documents authored by other colleagues.
* Providing guidance and training to less experienced medical writers and members of the wider team.
QUALIFICATIONS:
As Senior Regulatory and Medical Writer you will require:
* 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).
* 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.
BENEFITS:
Salary of up to £70,000 plus benefits package.
APPLY:
Please quote job reference in all correspondence.
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