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, and federal regulations including FDA CFR and ICH GCP.
The position requires effective collaboration with Principal Investigators, sponsors, and ancillary departments to support compliant study administration.
Matching Summary
The role involves contributing to the operational management of clinical research activities from design through closeout under direct supervision.
Salary
Hourly: $27.08 - $43.55; Range: $29.28 - $47.10; Not specified
Skills & Requirements
Must-have
Bachelor's degree in related area
2+ years study coordination experience
Knowledge of FDA CFR and ICH GCP regulations
Proficiency with Adobe and Microsoft Excel
Ability to manage competing deadlines
Nice-to-have
Compassionate patient interaction skills
Experience with multicenter clinical trials
Flexibility for travel between clinic sites
Strong verbal and written communication
Adaptability to changing job demands
Key Requirements
Bachelor's degree required
Minimum 2 years clinical research experience
Working knowledge of human safety protection regulations