Responsibilities:
- Produce wellwritten highquality timely Medical Writing documents (like Clinical Study Reports Protocols and amendments Investigators Brochure IB and IB updates etc)
- Review (including peer and QC review) Medical Writing documents in accordance with current SOPs ensuring checklists and tracking documents are completed
- Proofread and provide editorial support on documents produced by other departments in company or by clients if requested
- Provide oversight on Medical Writing projects and/or crossfunctional projects using project management tools and processes
- Manage the document review process ensuring conflicting and/or ambiguous comments are clarified and adequately addressed
- Assist Principal Medical Writers and above with the management of department budget and financials
- Actively contribute to business development by keeping CV uptodate preparing and reviewing client proposals and other business development documentation as well as presenting at client meetings and bid defense meetings
- Line manage assigned personnel taking an active role in their development and provide guidance and mentorship to less experienced Medical Writers
- Conduct literature reviews and provide input on the development of scientific communication and messaging
- Manage timelines and deliver documents within established deadlines
Requirements
- Masters degree or higher in a life science or related field.
- Minimum 5 years of experience as a Medical Writer in the pharmaceutical biotechnology or CRO industry.
- Strong knowledge of clinical research regulatory requirements and industry guidelines (ICHGCP).
- Excellent writing editing and proofreading skills with the ability to communicate complex scientific information effectively.
- Experience in writing clinical study documents such as protocols clinical study reports and regulatory submission documents.
- Detailoriented with excellent organizational and time management skills.
- Ability to work independently and collaboratively in a team environment.
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Remote Work :
No