Entry-Level Clinical Research Coordinator

Adams Clinical; Boston (MA); On-site; USD 77,366,000 - 91,693,000; Full time

Benefits offered by this job

401(k) matching

Medical, Dental & Vision insurance

Paid time off

Professional development assistance

Health savings account

Job summary

Adams Clinical in Boston, MA is seeking a Clinical Research Coordinator I to support and perform routine clinical research activities under guidance. The CRC I may independently manage lower-complexity trials and serves as a secondary coordinator on high-enrolling screening trials.

This role represents the first step in ownership of study execution. The ideal candidate has a Bachelor's degree and at least 6 months of industry-sponsored trial experience, with strong organization and a willingness

Qualifications

• Bachelor’s degree required and prior clinical research exposure preferred.
• Demonstrated ability to multitask and stay organized in a fast-paced setting.
• Willingness to learn hands-on clinical and research skills.

Responsibilities

• Coordinate low- to moderate-complexity trials, including visits and scheduling.
• Support screening, enrollment, and participant follow-up as secondary CRC on high-enrolling trials.
• Collect medical/psychiatric histories, vitals, and lab procedures per protocol.
• Prepare source documents, CRFs, and visit materials with ALCOA+-compliant records.
• Assist with IP accountability, storage, dispensing, and temperature monitoring.
• Communicate with participants between visits to maintain protocol adherence.
• Support sponsor communication, monitoring visits, and audit readiness.
• Contribute to data cleaning, study metrics, and reporting for inspections.
• Assist screening operations and help meet enrollment targets.

Skills

Organizational skills

Multitasking

Willingness to learn

Education

Bachelor’s degree required

6 months clinical research experience

Job description

Adams Clinical in Boston, MA is seeking a Clinical Research Coordinator I to support and perform routine clinical research activities under guidance. The CRC I may independently manage lower-complexity trials and serves as a secondary coordinator on high-enrolling screening trials.

This role represents the first step in ownership of study execution. The ideal candidate has a Bachelor's degree and at least 6 months of industry-sponsored trial experience, with strong organization and a willingness