Clinical Research Scientist
Job Summary
To support clinical trial initiatives, the full-time Clinical Research Scientist will develop study protocols, contribute to data management, and assist in regulatory document preparation while working remotely.
Key responsibilities
- Develop specific study concept sheets and protocols based on clinical trial design knowledge
- Prepare and review study protocols, amendments, and other necessary documentation with appropriate supervision
- Assist in the preparation of regulatory documents, including IND annual reports and Investigator Brochures
Required qualifications
- Bachelor's degree in a relevant field
- 8+ years of relevant scientific and/or drug development experience
- Experience in clinical trial design and data analysis
- Ability to summarize scientific information from published literature
- Excellent verbal and written communication skills
Complete Job Description
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