Clinical Research Coordinator — Trials & Compliance Pro

Bon Secours Mercy Health; Midlothian (VA); On-site; USD 37,000 - 57,000; Full time

Benefits offered by this job

Competitive pay

Medical, dental, vision coverage

403(b) with employer contributions

Paid time off and family leave

Tuition assistance and professional/CE

Job summary

Bon Secours Mercy Health seeks a regulatory affairs/clinical research professional to implement and manage components of active clinical trials, coordinating with legal, finance, and compliance teams. Responsibilities include consent handling, data capture, IRB submissions, SAE reporting, and tracking continuing reviews.

The role requires a Bachelor’s in health/science, 2+ years in regulatory affairs, and strong organizational and communication skills.

Qualifications

• Bachelor’s degree in a health science, life science, or related field.
• Minimum of 2 years of experience in regulatory affairs or clinical research.
• Familiarity with regulatory and ethical requirements related to human subjects research (IRB, FDA, ICH-GCP).
• Proficiency in Microsoft Office and familiarity with regulatory databases.

Responsibilities

• Implement and manage aspects of active clinical research programs and assist investigator providers as assigned.
• Handle consents, data capture, and regulatory submissions; manage SAE reporting to IRBs.
• Track annual reviews and continuing reviews; assist with amendments and safety reports.

Skills

Attention to detail

Regulatory knowledge

Communication skills

Time management

MS Office

Education

Bachelor’s degree in health science or related field

Master’s degree or regulatory certification (SOCRA/ACRP)

Tools

OnCore

REDCap

Job description

Bon Secours Mercy Health seeks a regulatory affairs/clinical research professional to implement and manage components of active clinical trials, coordinating with legal, finance, and compliance teams. Responsibilities include consent handling, data capture, IRB submissions, SAE reporting, and tracking continuing reviews.

The role requires a Bachelor’s in health/science, 2+ years in regulatory affairs, and strong organizational and communication skills.