Clinical Research Coordinator

Adams Clinical•New York City, NY

About The Position

Adams Clinical is a clinical trial site network focused on late-phase, industry-sponsored trials for psychiatric and neurological conditions, supporting both inpatient and outpatient studies. The Clinical Research Coordinator I works at the company’s Bronx research site and supports and performs routine clinical research activities under the guidance of a CRC II or CRC III. The role is suited to early-career coordinators with prior research exposure who want to build hands-on clinical and protocol-management experience. The coordinator may independently manage lower-complexity studies, such as maintenance and extension studies, and act as a secondary coordinator on high-enrolling screening trials. This position is an initial step toward greater ownership and accountability in study execution. Compensation is $27.00–$33.00 per hour.

Requirements

Bachelor’s degree.
At least 6 months of prior clinical research experience.
Strong organizational skills and ability to multitask in a fast-paced environment.
Willingness to continue learning hands-on clinical and research skills.

Nice To Haves

Experience with industry-sponsored clinical trials.

Responsibilities

Independently coordinate low- to moderate-complexity trials, including scheduling, visit execution, and day-to-day operations.
Serve as a secondary coordinator on high-enrolling screening trials, supporting screening, enrollment, and participant follow-up.
Conduct protocol-based participant visits, including medical and psychiatric history collection, vital signs, ECGs, phlebotomy, and specimen processing, as trained.
Prepare and maintain study source documents, lab kits, CRFs, and visit materials.
Maintain accurate, ALCOA+-compliant documentation of study procedures and maintain required logs, trackers, and regulatory files.
Support investigational product accountability for assigned studies under supervision, including receipt, storage, dispensing, reconciliation, temperature monitoring, and documentation, in accordance with protocols and site SOPs.
Communicate with participants between visits to maintain engagement and protocol compliance.
Assist with sponsor communication, monitoring visit preparation, and audit readiness as appropriate.
Contribute to query resolution, data cleaning, and study-metrics tracking to support accurate reporting and inspection readiness.
Support screening operations and meet enrollment expectations for assigned study tasks.
Prepare internal reports or summaries for review under the guidance of CRC II or CRC III.