Details:
- Job Type: Temporary
- Job Status: Full-Time
- Location: Nationwide
- Date: 5 days ago
Description:
Medical Writer
???? Location: Remote
✈️ Travel: Minimal (occasional team meetings and scientific conferences)
About the Role
As a Medical Writer, you will be responsible for developing high-quality clinical study documentation to support the company's medical products across a range of pre-market and post-market studies. Working closely with cross-functional teams, you'll play a key role in generating clinical evidence that supports both regulatory requirements and improved patient outcomes.
Key Responsibilities
Author clinical study protocols, clinical study reports, and other clinical investigation documentation.
Prepare clinical data summaries for internal stakeholders, healthcare professionals, patients, and regulatory authorities.
Ensure all documentation is developed in accordance with Good Clinical Practice (GCP).
Conduct literature reviews and database searches (PubMed, Embase) to support study design and evidence generation.
Collaborate with global teams across multiple business units.
About You
BSc with 3-5 years of relevant experience, or MSc/PhD with 1-2 years of relevant experience.
Proven experience writing clinical study documents, particularly protocols and clinical study reports.
Trained in Good Clinical Practice (GCP).
Excellent scientific and written communication skills.
Strong literature review and evidence assessment capabilities.
Experience with CTMS and eTMF systems is advantageous.
Knowledge of the medical device and/or pharmaceutical industry is preferred.
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy