Clinical Research Coordinator- San Antonio, TX (Temp to Perm)
About the role
IMA Clinical Research is seeking an experienced Clinical Research Coordinator for a temporary-to-permanent role in San Antonio, TX.
Responsibilities
- Coordinate clinical trials per protocol and SOPs
- Communicate with sponsors, CROs, CRAs, IRBs, and site staff
- Support investigators and ensure accurate documentation (ALCOA)
- Report adverse events and maintain study data integrity
Qualifications
- 2+ years of clinical research experience with phlebotomy
- Bachelor’s degree required (Master’s preferred)
- Ability to manage multiple studies independently
- CCRC certification a plus
Benefits (upon conversion)
- Medical, dental, vision insurance
- PTO, holidays, and floating holiday
- 401(k) with employer match
- Tuition reimbursement & student loan repayment assistance
- Paid parental leave
- No on-call responsibilities
Schedule
Not specified
Pay
Not specified
IMA Group Information
The IMA Group is an Affirmative Action/Equal Opportunity Employer. Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.