On-Site CNS Clinical Research Coordinator

PhaseWell Research; Toms River (NJ); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

401(k) with company match

Paid time off

Job summary

Bio Behavioral Health, a PhaseWell Research site, seeks a detail-oriented Clinical Research Coordinator (CRC) to support CNS trials. You will manage day-to-day study coordination, consent participants, support visits, maintain ALCOA+ source docs, and help ensure protocol adherence in a fast-paced, highly regulated environment.

On-site in Toms River, you will collaborate with investigators, sponsors, and monitors, while contributing to high-quality trial execution and data integrity.

Qualifications

• Bachelor's degree in life sciences, nursing, or related field.
• 1–3+ years clinical research experience typical.
• Knowledge of GCP, FDA regulations, and ICH guidelines.

Responsibilities

• Coordinate and conduct patient-facing study activities from site initiation through close-out.
• Screen, consent, and enroll participants from surrounding communities; support recruitment.
• Perform clinical procedures as trained (vital signs, sample handling).
• Maintain source documentation in ALCOA+ compliant systems.
• Track adverse events and IP accountability; report deviations per protocol.

Skills

GCP knowledge

Time management

Communication

Independent worker

Education

Life sciences degree

Tools

EDC systems

Microsoft Office

Job description

Bio Behavioral Health, a PhaseWell Research site, seeks a detail-oriented Clinical Research Coordinator (CRC) to support CNS trials. You will manage day-to-day study coordination, consent participants, support visits, maintain ALCOA+ source docs, and help ensure protocol adherence in a fast-paced, highly regulated environment.

On-site in Toms River, you will collaborate with investigators, sponsors, and monitors, while contributing to high-quality trial execution and data integrity.