Lead Clinical Research Coordinator: Trials & Compliance

Morehouse School of Medicine; Atlanta (GA); On-site; USD 70,000 - 110,000; Full time

Job summary

Morehouse School of Medicine is seeking a seasoned clinical research professional to manage substantial aspects of large trials or multiple smaller projects. The role involves staff training, data management oversight, participant interfaces, and ensuring protocol compliance across study activities.

Responsibilities include IRB monitoring, sponsor communications, and contributing to policy improvements. Depending on credentials, duties may include phlebotomy or diagnostics, with potential

Qualifications

• Knowledge of clinical research regulatory requirements (GCP/ICH).
• Proficiency in Microsoft Word, Excel and PowerPoint.
• Strong written and verbal communication skills.
• Excellent organizational and problem-solving abilities.
• Effective time management and prioritization of multiple tasks.

Responsibilities

• Independently manages significant aspects of a large clinical trial or all aspects of small trials.
• Trains and provides guidance to staff.
• Oversees data management for research projects.
• Interfaces with participants and resolves protocol issues.
• Authorizes purchases for supplies and equipment maintenance.
• Monitors IRB submissions and responds to requests and questions.
• Leads in proposing improvements to policies/processes.
• Assists in grant proposals and study protocols.
• May perform phlebotomy, specimen collection or diagnostics as trained.
• Performs supervisory duties as assigned.

Skills

GCP/ICH knowledge

MS Office

Written communication

Organizational skills

Time management

Education

High School Diploma or GED

Two years of college in scientific/health/business

Licensed Practical Nurse (LPN)

Bachelor's degree in scientific/health/business

Master’s degree, MD or PhD in scientific/health/business

Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC)

Job description

Morehouse School of Medicine is seeking a seasoned clinical research professional to manage substantial aspects of large trials or multiple smaller projects. The role involves staff training, data management oversight, participant interfaces, and ensuring protocol compliance across study activities.

Responsibilities include IRB monitoring, sponsor communications, and contributing to policy improvements. Depending on credentials, duties may include phlebotomy or diagnostics, with potential