Supports clinical research and compliance by partnering with senior team members to conduct reveiws, including preparation, implementation, closeout and reporting to ensure adherence to federal regulations and institutional policies. Interfaces with investigators, project managers, sponsors and staff during the review process. Will also lead in the development of consent forms, case report forms, checklists and other study documentation. Will mentor junior staff on good clinical practices in research.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees