Clinical Research Coordinator: Lead Complex Trials

Cenexelresearch; Savannah (GA); On-site; USD 34,440 - 39,950; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

LTD

STD

Life Insurance

401k

Job summary

CenExel Clinical Research in Savannah, GA, is seeking a skilled Clinical Research Coordinator to manage complex trials from initiation through closeout. You will ensure adherence to ICH/GCP, coordinate patient involvement, data collection, and regulatory duties, while collaborating with CTMs, sponsors, and vendors to drive quality and compliance.

The role requires 2–3 years in the medical field, regulatory knowledge, and strong communication.

Qualifications

• Must have experience and demonstrate mastery of a Clinical Research Coordinator position.
• High school graduate or equivalent; Bachelor's Degree preferred.
• CCRC certification preferred.
• 2‑3 years of experience in the medical field preferred.
• Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
• Strong leadership and mentorship skills.
• Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
• Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
• Works independently as well as functioning as part of a team.
• Must be able to effectively communicate verbally and in writing.

Responsibilities

• Coordinates aspects of patient involvement for complex and/or multiple studies from initiation to completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules the collection of data.
• Reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
• Monitors, and reports research data to maintain quality and compliance.
• Performs administrative and regulatory duties related to the study.
• Participates in other protocol development activities.
• Ensures site receives accurate information and supplies from sponsors.
• Educates potential participants and caregivers on protocol details and expectations.
• Performs safety and efficacy assessments per protocol.
• Assists Clinical Trial Manager (CTM) with oversight of vendors, accounting, regulatory, client satisfaction, recruitment, quality, and trial outcomes.
• Assists the CTM in planning, creating processes, trainings and development of staff.
• Assumes other duties and responsibilities as assigned.

Skills

Clinical Research Coordinator

Leadership

Communication

Crisis management

Regulatory knowledge

Education

High school diploma or equivalent

Bachelor's degree preferred

CCRC certification preferred

Job description

CenExel Clinical Research in Savannah, GA, is seeking a skilled Clinical Research Coordinator to manage complex trials from initiation through closeout. You will ensure adherence to ICH/GCP, coordinate patient involvement, data collection, and regulatory duties, while collaborating with CTMs, sponsors, and vendors to drive quality and compliance.

The role requires 2–3 years in the medical field, regulatory knowledge, and strong communication.