Job Description

🚨 Contract Opportunity – Clinical Research Coordinator I | Port Charlotte, FL (On-site) 🚨

We are seeking a highly skilled Clinical Research Coordinator for a 2–3 month contract role in Port Charlotte, Florida . This is an on-site opportunity ideal for an experienced clinical researcher with a passion for precision, protocol compliance, and patient-centered care.

🔍 About the Role:

As a CRC, you’ll work under the direction of the Principal Investigator and play a vital role in supporting all aspects of clinical trials, including patient interaction, data collection, regulatory compliance, and communication with Sponsors and CROs. You’ll be instrumental in study start-up, execution, and closeout.

🧠 Key Responsibilities:

• Conduct protocol-required visits, questionnaires, and study procedures
• Dispense/administer investigational products per protocol
• Engage with patients, PIs, Sponsors, and CROs
• Ensure GCP/ICH and ALCOA-compliant documentation and data entry
• Drive patient enrollment using EMR pre-screening
• Maintain accurate source documents, logs, CRFs, and reports
• Support AE/SAE reporting, study monitoring visits, and site audits
• Collect and process specimens, ECGs, and perform basic clinical tasks
• Travel to Investigator Meetings or other sites as needed

🎓 Qualifications:

• 3+ years of clinical research experience
• GCP and HSP Certified (must be current)
• Minimum 2 years as a Clinical Research Coordinator
• Bachelor’s degree in Nursing or Health Sciences preferred
• Experience in nephrology, CKD, or vascular access is a plus
• Bilingual (Spanish) preferred
• Comfortable with basic clinical procedures and ECGs
• Strong understanding of FDA regulations and IATA standards

🗓️ Contract Length: 2–3 months

📍 Location: On-site in Port Charlotte, FL

If you're looking to make an impact in clinical research while working with a dedicated team in a fast-paced, patient-focused environment, we want to hear from you!

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