Clinical Research Coordinator

Adams Clinical•New York, NY

2d•$27 - $33

About The Position

Adams Clinical is a growing clinical research site network focused on late-phase, industry-sponsored trials for psychiatric and neurological conditions, supporting inpatient and outpatient studies. The Clinical Research Coordinator I works at the company’s Bronx research site and is suited to an early-career coordinator with prior research exposure who wants to develop hands-on clinical and protocol management experience. Under the guidance of a CRC II or CRC III, this role supports and performs routine clinical research activities. The coordinator may independently manage lower-complexity trials, such as maintenance and extension studies, and serve as a secondary coordinator on high-enrolling screening trials. It is an initial step toward greater ownership and accountability in study execution.

Requirements

Bachelor’s degree required.
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 preferred.

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 participant visits according to protocol, including medical and psychiatric history collection, vital signs, ECGs, phlebotomy, and specimen processing, as trained.
Prepare and maintain study source documents, lab kits, case report forms (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 compliance with protocol 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/III.