Clinical Research Coordinator II: Lead Trials & Data

Morehouse School of Medicine; Atlanta (GA); On-site; USD 60,000 - 90,000; Full time

Job summary

Morehouse School of Medicine in Atlanta, GA is seeking a Clinical Research Coordinator II to independently manage significant aspects of one or more clinical trials, train staff, oversee data management, and interact with research participants to resolve issues related to study protocols. The role requires knowledge of GCP/ICH, strong organizational and communication skills, and proficiency in MS Office.

A Bachelor’s or higher degree in a scientific/health-related or business field is preferred,

Qualifications

• Knowledge of applicable clinical research regulatory requirements (GCP and ICH).
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Written and verbal communication skills.
• Excellent organizational and problem-solving skills.
• Effective time management and ability to manage competing priorities.

Responsibilities

• Independently manages significant and key aspects of one or more trials or research projects.
• Trains and provides guidance to less experienced staff.
• Oversees data management for research projects.
• Interacts with research participants and resolves issues related to study protocols.
• Authorizes purchases for supplies and equipment maintenance.
• Determines strategies for promoting and retaining participants in long-term trials.

Skills

GCP/ICH

MS Office

Communication skills

Organizational skills

Time management

Education

High School Diploma

Two years of college + 5 years of experience

Bachelor’s degree in scientific/health-related or business administration

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

Licensed as LPN

CRA or CRC certification preferred

Job description

Morehouse School of Medicine in Atlanta, GA is seeking a Clinical Research Coordinator II to independently manage significant aspects of one or more clinical trials, train staff, oversee data management, and interact with research participants to resolve issues related to study protocols. The role requires knowledge of GCP/ICH, strong organizational and communication skills, and proficiency in MS Office.

A Bachelor’s or higher degree in a scientific/health-related or business field is preferred,