Job Description
Your new company
Are you a detail-driven communicator with a passion for science and clinical research?
We're partnering with a leading global biopharmaceutical company-renowned for its innovation in rare disease therapies-to find a Medical Writer to join their Clinical Development team.
This is a fantastic opportunity for someone looking to grow their career in medical writing within a collaborative, science-led environment that values precision, clarity, and impact.
Your new role
As a Medical Writer, you'll play a key role in the development and delivery of high-quality clinical documentation that supports regulatory submissions and scientific publications.
You'll work cross-functionally with clinical teams, statisticians, and regulatory experts to ensure documents are accurate, compliant, and aligned with strategic goals.
Key Responsibilities:
Draft and edit clinical study documents including protocols, amendments, informed consent forms, and study reports
Contribute to safety and efficacy documentation such as Investigator's Brochures and periodic safety reports (PBRERs, DSURs)
Manage timelines, meetings, and review cycles for document development
Provide peer review and editing support across regulatory documentation
Support the development of templates and best practices within the medical writing functi...