Clinical Research Coordinator IV

Jobtailor; Atlanta (GA); On-site; USD 90,000 - 130,000; Full time

Job summary

Jobtailor in Atlanta, GA seeks an experienced Clinical Research Manager to lead research administration teams and oversee complex clinical trials, budgets, and regulatory compliance.

You will develop study materials, coordinate grants, train staff, and ensure adherence to protocols, with opportunities to drive process improvements and audits across programs.

Qualifications

• Master's or higher degree preferred with relevant clinical research experience.
• Clinical research leadership and budget oversight experience required.
• Experience ensuring regulatory compliance and quality in research operations.
• Experience in grant development and coordination is advantageous.

Responsibilities

• Recruits, orients, and supervises research administration staff or manages complex clinical trials.
• Manages large or multiple clinical research projects.
• Manages clinical trials information systems and study budgets.
• Ensures adherence to study protocols and CAP/Regulatory requirements.
• Educates staff on policies, processes and procedures.
• Develops and submits grant proposals and materials.
• Leads committees to address significant issues.

Skills

Leadership

Budget management

Regulatory compliance

Staff training

Quality assurance

Education

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

Bachelor's degree in scientific/health-related/business administration

Licensed Practical Nurse (LPN)

Two years of college in scientific/health-related/business administration

High School Diploma or GED

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

Job description

Responsibilities

• Recruits, orients, and supervises research administration staff or independently manages the most complex research administration activities associated with the conduct of clinical trials
• Manages a large or multiple smaller clinical research projects
• Manages clinical trials related information systems
• Supervises the implementation of and adherence to study protocols
• Monitors expenditures and adherence to study budgets and resolves CAS issues
• Educates research staff on established policies, processes and procedures
• Determines effective strategies for promoting/recruiting research participants and retaining participants in long‑term clinical trials
• Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes
• Plans, identifies, and handles study‑related equipment and facilities needs
• Provides leadership and expertise in identifying and completing research grants, study materials, brochures and correspondence
• Develops and submits grant proposals
• Leads or chairs committees or task forces to address and resolve significant issues
• Performs related approved responsibilities as required

Requirements

• High School Diploma or GED and nine years of clinical research experience
• Two years of college in a scientific, health‑related, or business administration program and seven years clinical research experience
• Licensed as a Practical Nurse (LPN) and six years clinical research experience
• Bachelor's degree in a scientific, health‑related, or business administration program and five years of clinical research experience
• Master's degree, MD or PhD in a scientific, health‑related, or business administration program and two years of clinical research experience
• Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred