Senior Medical Writer
4 weeks ago
About the Role
The Senior Medical Writer will be responsible for researching, creating, and editing all documents associated with clinical research. This includes protocols, clinical study reports, investigator's brochures, informed consent forms, and summary documents. The ideal candidate will have experience in regulatory medical writing and be able to operate as the project lead writer/submission coordinator and primary client contact.
Key Responsibilities
- Research and create high-quality medical documents
- Edit and revise documents to ensure accuracy and clarity
- Manage multiple projects and prioritize tasks effectively
- Collaborate with cross-functional teams to ensure seamless project execution
- Develop and maintain strong relationships with clients and stakeholders
Requirements
- 6+ years of experience in regulatory medical writing
- Experience in multiple therapeutic areas, including vaccines, immunology, autoimmune disorders, and more
- Strong communication and interpersonal skills
- Bachelor's/advanced degree in life sciences/healthcare
- Experience in the pharmaceutical/CRO industry
- Ability to work independently and lead projects
- Strong analytical skills
- Commitment to highest quality outputs
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