Clinical Research Coordinator I

About Us

Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is to deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. We specialize in late-phase industry-sponsored trials of novel treatments for psychiatric and neurological conditions, supporting both inpatient and outpatient studies across locations in Watertown, MA; Boston, MA; Harlem, NY; Bronx, NY; Philadelphia, PA; and Dallas, TX.

Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we foster a culture of respect, transparency, and continuous improvement. We offer opportunities for professional growth and learning in a team dedicated to improving lives through innovation and integrity.

Overview

We are seeking an experienced Clinical Research Coordinator I (CRC I) for our Boston location. This role is ideal for early-career coordinators with some prior research exposure, looking to develop hands-on clinical and protocol management experience. The CRC I supports routine clinical research activities under guidance and may independently manage lower-complexity trials while serving as a secondary coordinator on high-enrolling screening trials.

Responsibilities

• Independently coordinate low- to moderate-complexity trials, including scheduling, visit execution, and day-to-day operations.
• Serve as secondary CRC 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.
• Ensure accurate, ALCOA+-compliant documentation of all study procedures and maintain required logs, trackers, and regulatory files.
• Support investigational product (IP) accountability, including receipt, storage, dispensing, reconciliation, temperature monitoring, and documentation under supervision, ensuring 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.
• 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 guidance from CRC II/III.

Qualifications

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

Pay

$27.00 - $32.00 per hour

Benefits

• 401(k) matching
• Medical, dental, and vision insurance
• Employee assistance program
• Flexible spending account
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance