Adams Clinical
Clinical Research Coordinator I
Summary
Adams Clinical is a rapidly growing clinical trial site network focused on late-phase, industry-sponsored trials for psychiatric and neurological conditions. The Clinical Research Coordinator I supports and performs routine clinical research activities under guidance, helping execute studies with high data quality, safety, and participant engagement. This role is designed for early-career coordinators to build hands-on clinical and protocol management experience.
What you'll do
- Independently coordinate low- to moderate-complexity trials, including scheduling, visit execution, and day-to-day study operations.
- Serve as secondary coordinator on high-enrolling screening trials, supporting screening, enrollment, and participant follow-up.
- Conduct participant visits per protocol, including medical/psychiatric history collection, vitals, ECGs, phlebotomy, and specimen processing (as trained).
- Prepare and maintain study source documents, lab kits, CRFs, and visit materials.
- Maintain accurate ALCOA+-compliant documentation, and keep required logs, trackers, and regulatory files.
- Support investigational product accountability (receipt, storage, dispensing, reconciliation, temperature monitoring, and documentation) under supervision per protocol and site SOPs.
- Communicate with participants between visits to support engagement and protocol compliance.
- Assist with sponsor communication, monitoring visit preparation, and audit/inspection readiness as needed.
- Contribute to query resolution, data cleaning, and study metrics tracking for accurate reporting.
- Support screening operations and meet enrollment expectations for assigned study tasks.
- Prepare internal reports or study summaries for review under CRC II/III guidance.
Requirements
Bachelor's degree required.
At least 6 months of prior clinical research experience; industry-sponsored clinical trial experience preferred.
Strong organizational skills and ability to multitask in a fast-paced environment.
Willingness to continue learning hands-on clinical and research skills.
Conditions
Pay range: $27.00–$33.00 per hour.
Benefits may include 401(k) matching, medical/dental/vision insurance, employee assistance program, flexible spending account, health savings account, life insurance, paid time off, parental leave, and professional development assistance.
Must be authorized to work in the United States and complete Form I-9; employer participates in E-Verify.