Clinical Research Coordinator I — Launch Your Trial Career

Adams Clinical, Inc.; New York (NY); On-site; USD 37,000 - 45,000; Full time

Benefits offered by this job

401(k) matching

Employee assistance program

Flexible spending account

Health insurance

Health savings account

Life insurance

Paid time off

Parental leave

Job summary

Adams Clinical is seeking a Clinical Research Coordinator I for our Bronx site, focused on late-phase, industry-sponsored trials in psychiatric and neurological conditions. This role is ideal for early-career coordinators with some research exposure seeking hands-on protocol management experience.

The CRC I coordinates visits, collects histories and vitals, prepares study materials, and supports IP accountability under supervision, building ownership in study execution and data quality.

Qualifications

• At least 6 months of prior clinical research experience; industry trials preferred.
• Strong organizational skills and ability to multitask in a fast-paced environment.
• Willingness to continue learning hands-on clinical and research skills.

Responsibilities

• Coordinate low- to moderate-complexity trials, scheduling visits and daily operations.
• Support high-enrolling screening trials as secondary CRC and assist with enrollment.
• Conduct participant visits per protocol including vitals and phlebotomy as trained.
• Prepare source documents, lab kits, CRFs, and visit materials.
• Ensure ALCOA+-compliant documentation and maintain logs/regulatory files.
• Assist IP accountability including receipt, storage, dispensing, and temp monitoring.
• Communicate with participants between visits to ensure protocol adherence.
• Support sponsor communications, monitoring prep, and audits.
• Contribute to data cleaning and study metrics tracking.

Skills

Organizational skills

Multitasking

Willingness to learn

Job description

Adams Clinical is seeking a Clinical Research Coordinator I for our Bronx site, focused on late-phase, industry-sponsored trials in psychiatric and neurological conditions. This role is ideal for early-career coordinators with some research exposure seeking hands-on protocol management experience.

The CRC I coordinates visits, collects histories and vitals, prepares study materials, and supports IP accountability under supervision, building ownership in study execution and data quality.