Senior Medical Writer - Clinical Operations
Core
Prepare clinical study documents (protocols, reports, data summaries) to support Convatec medical products across pre- to post-market studies.
Role type
Senior Medical Writer (Clinical Operations)
Builds
Clinical study protocols, study reports, and data summaries for regulatory authorities and internal teams.
Domain
Medical device / Pharmaceutical industry
Required skills
Clinical study document writing, Good Clinical Practice (GCP), Literature search and review, Protocol development, Data summarization
Preferred skills
CTMS, eTMF, Medical device/pharmaceutical industry knowledge, Embase, PubMed
Technologies
CTMS, eTMF, Embase, PubMed
Responsibilities
Develop protocols, study reports, and clinical investigation materials; Prepare data summaries for internal and external audiences; Implement Good Clinical Practice in document development; Perform literature searches to support study design and strategic decisions; Stay current on registered studies and published literature.
Seniority
Senior, hands-on IC
