As part of our on-going growth, we are currently recruiting for a Senior Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific.
The Phase II-IV Medical Writing group, which is part of the Biostatistics Department, includes Writers who prepare documents in support of clinical trials and who assist Regulatory Affairs professionals with marketing applications, INDs, paediatric investigational plans, clinical trial applications, and other types of regulatory documents.
The Medical Writer collaborates with internal and sponsor team members to interpret, distil, and summarize complex data concepts. Other tasks include presentation of clinical messages in clinical study reports, summarization of preclinical and clinical studies for preparation of investigator's brochures, and referencing current research and regulatory guidelines for preparation of protocols. Their work documenting clinical study trials covers a wide range of therapeutic indications. Qualifications
Education to Bachelor's/advanced degree level in a scientific discipline Prior experience within regulatory medical writing Excellent grammatical, editorial and proofreading skills Effective organisational and planning skills Motivation, initiative and adaptability Ability to work effectively in a teamThe successful candidates can look forward to job stability with a leading CRO that has experienced year-on-year growth. We offer a generous salary and benefits package as well as excellent learning and development opportunities. We understand that the best writers are not necessarily on our doorstep, so if you are looking for a home based role we can offer this option to the right candidate, providing everything you need to fulfil your potential from your home office.