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 in an apprenticeship role assisting experienced medical writers at Trilogy. Producing regulatory documents for pharmaceutical companies in a dynamic and diverse team environment.
Responsibilities
- Work alongside experienced medical writers, supporting the production of regulatory documentation for the international pharmaceutical industry
- Assist in writing and coordinating regulatory documents across a broad spectrum of therapeutic areas
- Participate in clinical development teams and provide integral writing support for regulatory submission packages
Requirements
- Bachelor’s degree in science/pharmacy (PhD not necessary) or equivalent
- Excellent written and spoken English skills
- A passion for writing and an eye for detail
- Well-developed, proven interpersonal skills and a proactive nature that enjoys participating on a team with diverse personalities
- Flexibility and the ability to stay focused under tight timelines across multiple time zones
Benefits
- Competitive base salary (range: $85,000 - $90,000 USD; the salary range is an estimate and may vary based on experience level, region, and the Company’s compensation practices)
- Annual bonus opportunity
- A generous allowance of paid time off (vacation, holiday, birthday, illness)
- Comprehensive benefit plans to include medical, dental, vision, disability, life insurance with AD&D
- 401K retirement savings plan with company match
- Full AMWA membership and annual conference attendance paid for by Trilogy
- Continuous personal and professional development opportunities
- Free weekly yoga sessions
- Other fun and exciting events that encourage team bonding and development
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