Clinical Trial Coordinator & Project Lead (Hybrid)

RiseMe; Raleigh (NC); Hybrid; USD 60,000 - 80,000; Part time

Job summary

Science 37 is seeking a Clinical Research Coordinator to recruit, enroll and follow up with study participants under the supervision of the Principal Investigator and Project Manager. You will coordinate trial participation in line with SOPs, GCP/ICH and FDA regulations, ensuring enrollment goals and protocol compliance.

This contract role has potential to convert to full-time after 6 months and may involve hybrid on-site/trial activities, requiring strong organization and communication across

Qualifications

• Bachelor’s degree preferred; 5+ years of pharma-sponsored clinical research experience is required or equivalent.
• Advanced degree preferred but not required.

Responsibilities

• Actively participates in planning, execution and closeout of clinical trial activities.
• Enlists, maintains, and assures protocol compliance for all study participants.
• Screens and enrolls participants and conducts informed consent.
• Maintains data collection, documentation and reporting with QA.

Skills

Trial management

FDA regulations

GCP guidelines

Communication

Leadership

MS Office

Education

Bachelor’s degree (preferred)

Two-year college degree minimum

Tools

MS Office

Google Suite

Job description

Science 37 is seeking a Clinical Research Coordinator to recruit, enroll and follow up with study participants under the supervision of the Principal Investigator and Project Manager. You will coordinate trial participation in line with SOPs, GCP/ICH and FDA regulations, ensuring enrollment goals and protocol compliance.

This contract role has potential to convert to full-time after 6 months and may involve hybrid on-site/trial activities, requiring strong organization and communication across