Clinical Research Coordinator II

Adams Clinical is a clinical trial site network specializing in late-phase industry-sponsored trials for psychiatric and neurological conditions. The Clinical Research Coordinator II independently manages complex or high-enrolling clinical trials, oversees study operations and participant visits, supports study start-up, and maintains data quality and inspection readiness. The role also serves as a liaison with sponsors, monitors, and CROs and may supervise junior research staff.

Responsibilities

Independently manage a portfolio of complex and/or high-volume trials with guidance from a CRC III or the Site Manager, leading all operational and visit-related activities

Fully own study execution, including screening operations, enrollment progress, screening vs. target metrics, and SCF rates

Conduct all participant visits, clinical procedures, and eligibility assessments per protocol

Lead study start-up activities for assigned studies, including SIV preparation, regulatory readiness, supply planning, and supporting site completion of required staff training

Serve as the primary liaison with study sponsors, monitors, and CROs

Review source and eligibility criteria to ensure accurate screening and enrollment decisions

Train and supervise CRC I's or RA's supporting the portfolio; maintain quality and performance oversight

Lead data entry and query resolution efforts, ensuring high data quality and inspection readiness

Maintain investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal, ensuring compliance with protocol, regulatory requirements, and site SOPs

Identify operational risks and propose corrective actions to maintain study timelines and quality

Compile study metrics across assigned trials, including enrollment progress, screening performance, visit completion, and data quality

Prepare internal performance summaries for the site team and escalate issues or trends to senior staff

Present study metrics and operational updates to sponsors, monitors, or CRO leadership for assigned trials

Serve as a point of contact for resolving data queries and ensuring inspection readiness

Benefits

401(k) matching

Medical, Dental, & Vision insurance

Employee assistance program

Flexible spending account

Health insurance

Health savings account

Life insurance

Paid time off

Parental leave

Professional development assistance

Company

US clinical research sites for psychiatric and neurological trials

Watertown, Massachusetts, USA

https://www.adamsclinical.com/

Founded in 2011

201-500 employees

Qualifications

Bachelor's degree required

At least 1 year of prior clinical research experience

Experience with industry-sponsored clinical trials required

Demonstrated ability to manage complex studies independently

Strong communication skills and comfort interacting directly with sponsors

At least 1 year of prior clinical research experience.

Required skills

Clinical Research, Industry-Sponsored Clinical Trials, Clinical Trial Management, Clinical Procedures, Study Start-Up, Regulatory Compliance, Investigational Product Accountability, Clinical Data Management

Experience

1+ years