The Clinical Research Supervisor oversees routine research coordination and unit operations to ensure strict compliance with policies and federal regulations
Job Summary
The Clinical Research Supervisor oversees routine research coordination and unit operations to ensure strict compliance with policies and federal regulations.
This role manages clinical studies from start-up through closeout while serving as a liaison between the Principal Investigator, internal teams, and sponsors.
Candidates must demonstrate advanced knowledge of FDA processes, human safety protection regulations, and the ability to manage complex departmental priorities.
Matching Summary
The Clinical Research Supervisor oversees routine research coordination and unit operations to ensure strict compliance with policies and federal regulations.
Salary
Base: $86,400 - $184,800 annually; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
5+ years clinical research experience
FDA CFR and ICH GCP knowledge
IRB and regulatory committee interaction
Clinical trials budgeting proficiency
Microsoft Excel and Adobe software skills
Nice-to-have
Compassionate patient communication
Flexible work schedule adaptability
Team leadership and presentation skills
Quality improvement initiative development
Collaborative relationship building
Key Requirements
Bachelor's degree required; Master's preferred
Minimum 5 years in clinical research setting
Experience with IRBs and scientific review committees