Clinical Documentation Specialist responsible for receiving and processing healthcare documentation requests. Analyzing and validating requests while ensuring compliance with regulations and organizational standards.
About the role
- Associate Medical Writer coordinating medical communication materials and ensuring high-quality content. Collaborating with teams while managing projects and conducting in-depth research on therapeutic areas.
Responsibilities
- Support the scientific team by drafting and preparing a variety of medical communication materials
- Ensure all content meets high standards of grammatical and scientific accuracy
- Fact-check, incorporate internal and external feedback
- Adapt to client preferences in writing style and terminology
- Manage assigned projects to meet deadlines
- Collaborate with scientific and client services colleagues
- Conduct in-depth research on therapeutic areas, competitors, and products
- Track time accurately against project budgets
- Maintain proficiency with relevant software
- Stay informed on compliance requirements and industry best practices
Requirements
- A life sciences degree, ideally combined with a science Masters or PhD
- Strong communication skills
- Good knowledge of pharmaceutical industry and processes
- Excellent attention to detail and organisational skills
- Good working knowledge of standard computer software e.g. Microsoft Office, Adobe, Excel
Benefits
- 33 days annual leave
- Birthday day off
- 5% pension contribution
- Private medical health insurance
- WORKsmart - allows employees to have flexibility around their start and finish time
- Hybrid working
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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