Clinical Research Scientist
Job Summary
Working remotely on a contract basis, the Clinical Research Scientist will develop study protocols, participate in protocol review discussions, and prepare regulatory documents while collaborating with team members in a flexible schedule environment.
Key responsibilities
- Develop specific study concept sheets and protocols based on clinical trial design
- Prepare study protocols, amendments, and regulatory documents with appropriate guidance
- Contribute to the design and development of CRFs, Data Management Manuals, and Data Analysis Plans
Required qualifications
- PharmD with 2+ years of relevant scientific and/or drug development experience
- MS with 6+ years of relevant scientific and/or drug development experience
- BS or RN with 8+ years of relevant scientific and/or drug development experience
Complete Job Description
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