Celerion is hiring a Medical Writer to join our team. In this role, you will be responsible for developing high-quality clinical and regulatory documents that support our research programs. This is a remote position for candidates based in the United States.
What You'll Do
- Author, review, and finalize clinical study protocols, study reports, and regulatory submission documents.
- Ensure all documents comply with regulatory guidelines, ICH requirements, and internal standards.
- Collaborate with cross-functional teams to gather information and ensure document accuracy.
- Manage timelines for document deliverables to meet project milestones.
What We're Looking For
- Proven experience writing clinical and regulatory documents for the pharmaceutical or biotechnology industry.
- Strong knowledge of ICH, GCP, and other relevant regulatory guidance.
- Excellent writing, editing, and attention to detail.
- Ability to work independently and manage multiple projects in a remote environment.
Work Mode
This is a fully remote position open to candidates residing in the United States.
Celerion is an equal opportunity employer.
