Clinical Research Project Coordinator I — Study Operations

Women & Infants Hospital; Providence (RI); On-site; USD 52,000 - 68,000; Full time

Job summary

Women & Infants Hospital in Providence, RI seeks a Clinical Research Project Coordinator I to oversee non-clinical administrative tasks for human subject research. You will coordinate daily project activities, liaise with the Principal Investigator, sponsor and junior staff, and help recruit participants and collect data in line with study protocols.

Responsibilities include maintaining study records, supporting IRB submissions, and ensuring compliance with regulatory requirements while

Qualifications

• Bachelor’s Degree required.
• Minimum 1–3 years experience.
• CCRP, CCRA, or ACRP-CP preferred.
• Excellent communication skills and analytic abilities.
• Basic computer skills, e.g. familiarity with Microsoft software and data entry.

Responsibilities

• Supervision and non-clinical administrative support for research projects.
• Coordinate daily activities of the project and act as contact for PI, sponsor, and junior staff.
• Initiate and maintain participant recruitment, track participants, and facilitate data collection.
• Ensure completion of study procedures and adherence to protocols.
• Maintain study records and assist with IRB and regulatory submissions.

Skills

Excellent communication skills

Analytic abilities

Microsoft software

Diversity and inclusion awareness

Education

Bachelor’s Degree

Job description

Women & Infants Hospital in Providence, RI seeks a Clinical Research Project Coordinator I to oversee non-clinical administrative tasks for human subject research. You will coordinate daily project activities, liaise with the Principal Investigator, sponsor and junior staff, and help recruit participants and collect data in line with study protocols.

Responsibilities include maintaining study records, supporting IRB submissions, and ensuring compliance with regulatory requirements while