Clinical Research Coordinator: Trials, Compliance & Impact

CenExel; Decatur (GA); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Health Insurance

Dental Insurance

Vision Insurance

LTD

STD

Life Insurance

401k

Job summary

CenExel is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials in accordance with ICH/GCP and company policies. The role emphasizes patient involvement, data collection, and regulatory compliance within a Georgia site.

Ideal candidates have CCRC certification and 2–3 years in the medical field, with strong communication and leadership abilities to support multiple studies and vendors.

Qualifications

• Must have proper experience and demonstrate mastery of Clinical Research Coordinator I position.
• Knowledge of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
• Strong leadership and mentorship skills.

Responsibilities

• Coordinates aspects of patient involvement for complex studies from initiation to completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules data collection and ensures timely reporting.
• Monitors and reports adverse events and protocol deviations.
• Assists CTM with oversight of vendors, regulatory, and recruitment activities.
• Educates participants and caregivers on protocol details and expectations.

Skills

Clinical Research

Verbal and Written Communication

Leadership

Education

CCRC certification

Job description

CenExel is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials in accordance with ICH/GCP and company policies. The role emphasizes patient involvement, data collection, and regulatory compliance within a Georgia site.

Ideal candidates have CCRC certification and 2–3 years in the medical field, with strong communication and leadership abilities to support multiple studies and vendors.