Clinical Research Coordinator

alcanzaclinical; Clearwater (FL); On-site; USD 52,000 - 78,000; Full time

Job summary

Alcanza is seeking a Clinical Research Coordinator to join our Florida team. The CRC will help execute assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs, supporting study sites across phases I–IV.

Ideal candidates are detail-oriented, capable of coordinating activities with investigators, staff, and vendors, and ensuring data integrity and participant safety throughout the study lifecycle in a multi-site environment.

Qualifications

• Experience coordinating clinical studies or site activities.
• Knowledge of GCP, ICH, HIPAA and FDA regulations is preferred.

Responsibilities

• Execute assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

Job description

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.