Medical Writer
Core
Lead and contribute to medical writing projects, authoring and quality-checking regulatory and scientific documents for clinical development programmes.
Role type
Senior Medical Writer (Consultant)
Builds
Regulatory and scientific documents (e.g., clinical study reports) for pharmaceutical and biotech clients
Domain
Life Sciences / Clinical Development / Regulatory Affairs
Deliverable
client delivery
Required skills
Medical writing, regulatory document preparation, project management, stakeholder management, mentoring, scientific communication, quality control, document publishing
Preferred skills
PhD/MD/PharmD, peer-reviewed publications, advanced scientific discipline background
Technologies
Microsoft Office, document management systems
Responsibilities
Author and review regulatory/scientific documents, manage multiple writing projects, serve as client point of contact, mentor junior writers, stay current with regulatory requirements
Seniority
Senior, hands-on IC with mentorship responsibilities
