Clinical Research Regulatory Coordinator

Prisma Health; Greenville (SC); On-site; USD 60,000 - 85,000; Full time

Job summary

Prisma Health in Greenville Memorial Hospital is seeking a regulatory professional to prepare, submit, and oversee diverse regulatory documentation for research projects. You will coordinate requirements, support faculty and staff in collaborations, and act as a subject-matter expert during audits.

Requirements include a Bachelor’s degree in a related field and five years of research/regulatory experience, with Clinical Research Certification preferred.

Qualifications

• Bachelor's degree in Biology, Nursing, Business, or Social Sciences related field of study.
• Five (5) years of research, Clinical Research, Regulatory‑clinical or industry experience.
• Three (3) years of related experience may be accepted if certified with CCRA or CCRP or Master's degree in related field of study.
• Clinical Research Certification preferred

Responsibilities

• Prepares, submits, and assists with regulatory documentation for research.
• Participates in planning and project management of studies.
• Serves as a regulatory expert within the department.
• Oversees regulatory requirements for research; ensures timely submission to committees.
• Leads quality improvement initiatives related to regulatory compliance.
• Maintains training records for the research team.
• Educates the team on regulatory issues through presentations and literature.
• Performs other duties as assigned.

Skills

Regulatory interpretation

Organizational & project management

Lead without authority

Attention to detail

Collaboration & service orientation

Education

Bachelor's degree in Biology, Nursing, Business, or Social Sciences

Job description

Prisma Health in Greenville Memorial Hospital is seeking a regulatory professional to prepare, submit, and oversee diverse regulatory documentation for research projects. You will coordinate requirements, support faculty and staff in collaborations, and act as a subject-matter expert during audits.

Requirements include a Bachelor’s degree in a related field and five years of research/regulatory experience, with Clinical Research Certification preferred.