Clinical Research Coordinator II — Advanced Trials

CenExel Clinical Research; Atlanta (GA); On-site; USD 50,000 - 65,000; Full time

Job summary

CenExel ACMR is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials from initiation to completion in a rigorous, compliant environment.

Responsibilities include organizing trial data, scheduling collections, monitoring safety metrics, and supporting regulatory tasks. Applicants should have 2–3 years of medical field experience and a Bachelor’s degree preferred, with CCRC preferred. On-site role with travel may be required.

Qualifications

• Must have mastery of Clinical Research Coordinator I duties.
• Bachelor’s degree preferred; CCRC certification preferred.
• 2–3 years experience in the medical field preferred.
• Knowledge of Federal regulations protecting human subjects in research.
• Strong leadership and mentorship skills are essential.
• Ability to build relationships across levels, sponsors, and vendors.
• Crisis management and problem-solving skills; work well under pressure.
• Effective written and verbal communication essential.

Responsibilities

• Coordinate patient involvement from study initiation to completion.
• Organize research information for clinical trials.
• Observe subjects and assist with data analysis and reporting.
• Schedule data collection activities.
• Review and report adverse events and protocol deviations.
• Monitor data quality and regulatory compliance.
• Perform administrative and regulatory duties related to the study.
• Participate in protocol development activities as needed.
• Ensure Sponsors provide accurate information and supplies.

Skills

Leadership

Mentorship

Teamwork

Communication

Education

Bachelor’s degree preferred

CCRC certification preferred

High school diploma or equivalent

2–3 years medical field experience preferred

Job description

CenExel ACMR is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials from initiation to completion in a rigorous, compliant environment.

Responsibilities include organizing trial data, scheduling collections, monitoring safety metrics, and supporting regulatory tasks. Applicants should have 2–3 years of medical field experience and a Bachelor’s degree preferred, with CCRC preferred. On-site role with travel may be required.