Dynamic Clinical Research Project Coordinator I

Care New England; Pawtucket (RI); On-site; USD 52,000 - 65,000; Full time

Job summary

Care New England Health System in Pawtucket, RI seeks a Clinical Research Project Coordinator I to supervise project staff, initiate and maintain recruitment, manage daily operations, and track progress of study participants, ensuring data required by sponsors is accurate and timely.

You will support IRB submissions and amendments, assist with regulatory reports, promote the project through marketing and website updates, coordinate meetings, and foster an inclusive, compliant environment across

Qualifications

• Bachelor's degree required; 1–3 years of experience preferred.
• CCR P, CCRA, or ACRP-CP preferred.
• Strong communication and analytical abilities are essential.
• Basic computer skills including MS Office and data entry.

Responsibilities

• Supervise project staff (CRAs, assistants, volunteers, students, consultants) and address HR issues as needed.
• Plan, implement, and manage project data.
• Promote the project through marketing, website, and other sources.
• Coordinate project meetings, create agendas and draft minutes.
• Collaborate on presentations, publications, and dissemination of results.
• Oversee biospecimen collection, packaging, shipping, and infection control procedures.
• Assist in preparing IRB protocols, amendments, reviews, risk assessments, adverse event reports, and informed consent documents; communicate with IRB throughout submission and review.
• Support investigators in preparing regulatory reports, DSMB meetings and NIH RPPRs.

Skills

Communication skills

Analytical abilities

Diversity & inclusion

Education

Bachelor's Degree

Tools

Microsoft Office

Excel

Data entry

Job description

Care New England Health System in Pawtucket, RI seeks a Clinical Research Project Coordinator I to supervise project staff, initiate and maintain recruitment, manage daily operations, and track progress of study participants, ensuring data required by sponsors is accurate and timely.

You will support IRB submissions and amendments, assist with regulatory reports, promote the project through marketing and website updates, coordinate meetings, and foster an inclusive, compliant environment across