About the job

Join Us in Shaping the Future of Clinical Research

Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change.

At Adams Clinical, you’ll find:

• A culture of respect, transparency, and continuous improvement
• Opportunities for professional growth and learning
• A team dedicated to improving lives through innovation and integrity
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If you’re passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we’d love to have you on our team.

Overview

Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions, supporting both inpatient and outpatient studies. Adams Clinical Site Network has locations in Watertown, MA; Boston, MA; Harlem, NY; Bronx, NY; Philadelphia, PA; and Dallas, TX.

We are seeking experienced applicants for the Clinical Research Coordinator I role at 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 Clinical Research Coordinator I is responsible for supporting and performing routine clinical research activities under the guidance of a CRC II or CRC III. The CRC I may independently manage lower-complexity trials (e.g., maintenance studies, extension studies) and serves as a secondary coordinator on high-enrolling screening trials. This role represents the first step in assuming ownership and accountability in study execution.

Key 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 for assigned studies, 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 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 guidance from CRC I
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