Are you an experienced CRC looking for your next project? This is a great opportunity to work with an award winning SMO, conducting multi-therapeutic clinical trials in phases I-IV.

Important Information:

• Location: Must reside locally in Edgewater, FL 32132
• Contract Duration: 5-6 months, support wrap up by end of January 2025; contract duration is subject to change
• Schedule: FULL TIME, 40 hours per week
• Clinic is open Monday-Friday 8:00am-5:00pm
• CRC will be administering the IP and performing bloods draws - MUST be licensed (Open to CMA or an LVN/LPN)

Responsibilities
● Perform overall data management of studies - collect, enter, and maintain records for clinical study subjects.
● Support accurate and timely data entry in electronic databases.
● Ensure all protocol-required procedures and visits occur according to specified guidelines.
● Manage participant enrollment and ensure compliance with the protocol during participant recruitment, informed consent, participant education, eligibility assessment, participant care, and follow-up per protocol.
● Collaborates with quality assurance (QA) in the development of source documentation for new studies, assisting in the assessment of toxicities/adverse events and reporting serious adverse events per IRB and sponsor requirements.
● Possess excellent interpersonal skills and collaborative with the research team.
● Independently manage workflows and prioritize numerous tasks.
● Be flexible and anticipate timeframes to accommodate frames subjects, monitors, and overtime hours during high-enrolling study periods.
● Maintains GCP certification and IATA training as required.
● Performs other duties as assigned.