Highlights:

• $23.00/Hr. - $26.00/Hr. Excellent benefits
• Full-Time, M-F schedule on-site
• Fast growing company with tons of opportunity!

**This is an on-site position, M-F, in the Little Havana area of Miami, FL. Please do not apply if you are seeking Hybrid or Remote**

The Company:

Our client is a clinical research site network organization that has a proven track record of success in clinical research. over 17 research sites across the seven states. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. They have plans to grow to 30 sites within about a year. They have partnership with a vast network of community based physicians and they make it easier for diverse patient populations to participate in clinical trials and by consistently delivering reliable results & quality data. They are on track to become one of the largest site networks in the country!

The Role:

You will be responsible for daily, patient-facing responsibilities / clinical support, reporting, and back-office support for assigned studies.

The most successful candidate for this opportunity will have experience in all facets of a research study. Start-up to close-out, phase I - IV, (phlebotomy experience not necessary, but a PLUS!) and able to handle multiple studies at a time.

• Conducts assigned studies (2 - 5 at a time generally) according to protocol & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines.
• Scheduling and Screening of patients for study enrollment, consents, follow-ups
• Patient recruitment as needed
• Documenting charts entering data in EDC and answering queries
• Obtaining vital signs, ECGs, and lab procedures
• Maintaining & ordering study specific supplies;
• Conducting monitoring visits, Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs)
• Filing SAE/Deviation reports to Sponsor and IRB; Handles all IRB functions
• Documenting and reporting adverse events
• Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF

Requirements:

• 2 years experience as a Clinical Research Coordinator for sponsor backed clinical research trials
• Bilingual in Spanish/English