Clinical Document Specialist
1 day ago
We are looking for a talented Clinical Document Specialist to join our team at Life Sciences Recruitment. As a key member of our content creation team, you will be responsible for preparing high-quality clinical regulatory documents, including Clinical Study Protocols, Clinical Study Reports, and Investigator Brochures.
Key Responsibilities:- Prepare clinical regulatory documents, working closely with client authoring teams and other writers.
- Ensure document quality, meet timelines, and manage project budgets while adhering to SOPs and client requirements.
- Work collaboratively with clients and internal teams to deliver high-quality documents.
The estimated salary for this role is around $90,000 - $120,000 per year, depending on experience.
Requirements:- A minimum of 3 years of experience in medical writing.
- Experience working with clinical regulatory documents and interacting with clients.
- Excellent communication and project management skills.
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Clinical Regulatory Document Specialist
1 day ago
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