The position involves coordinating clinical assessments of study subjects under minimal supervision. The individual will analyze and assist in interpreting moderately complex clinical research data. Additionally, the role includes preparing grant applications and documents, as well as assisting in protocol submissions to relevant bodies such as the Institutional Review Board and Grants and Contracts Office.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Number of Employees
5,001-10,000 employees