Lead Clinical Research Coordinator

Eximia Research; Florida; On-site; USD 45,000 - 65,000; Full time

Job summary

Eximia Clinical Research is seeking a Clinical Research Coordinator to manage trials from start-up to close-out in accordance with protocol, GCP, and SOPs. You will serve as the subject matter expert and lead study execution, while training staff and coordinating regulatory documents.

The role requires strong knowledge of clinical trial processes, data integrity, and effective communication with sponsors, CROs, and vendors while maintaining patient safety and ALCOA-C data practices.

Qualifications

• Bachelor’s degree with 6 years as CRC or Associate’s with 8 years or High School/technical with 10 years of CRC experience.
• Phlebotomy if applicable and required by state law
• ACRP or SOCRA CRC certification within six months of role start
• Proficient use of medical terminology and MS Office; strong organizational skills.

Responsibilities

• Serve as lead of studies to execute clinical trials.
• Train staff in the conduct of clinical trials, protocol requirements, communication.
• Conduct and manage clinical trials in accordance with protocol, GCP, and SOPs.
• Perform venipuncture, sample processing, and lab specimen handling as required.
• Coordinate trials including start up, vendor management, regulatory documents, and ICF processes.
• Ensure data entry, reporting of adverse events, and close-out reports per protocol.

Skills

Medical terminology

Communication

Team leadership

Fast-paced work

Education

Bachelor’s degree + 6 yrs CRC

Associate’s degree + 8 yrs CRC

High School + 10 yrs CRC

Tools

MS Office

Computers

Job description

Eximia Clinical Research is seeking a Clinical Research Coordinator to manage trials from start-up to close-out in accordance with protocol, GCP, and SOPs. You will serve as the subject matter expert and lead study execution, while training staff and coordinating regulatory documents.

The role requires strong knowledge of clinical trial processes, data integrity, and effective communication with sponsors, CROs, and vendors while maintaining patient safety and ALCOA-C data practices.