The role involves contributing to the operational management of clinical research activities from design through closeout under direct supervision
Job Summary
The role involves contributing to the operational management of clinical research activities from design through closeout under direct supervision.
Candidates must ensure adherence to study protocols, institutional policies, FDA Code of Federal Regulations, and ICH Good Clinical Practice.
The position requires effective collaboration with Principal Investigators, ancillary departments, sponsors, and regulatory committees to support study administration.
Matching Summary
The role involves contributing to the operational management of clinical research activities from design through closeout under direct supervision.