Clinical Research Coordinator

Flourish Research • Fleming Island, FL

3d • $21 - $28 • Onsite

About The Position

Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.

We are actively hiring Clinical Research Coordinators at our Fleming Island, FL site location! This site has provided clinical research opportunities to residents in the Fleming Island, Green Cove Springs, and Middleburg communities since 2009!

The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction.

Requirements

• Bachelor's degree preferred, but not required
• Clinical skills highly preferred: vital signs, phlebotomy, ECG/EKG, injections, etc
• Preferably 2+ years of experience as a Clinical Research Coordinator
• Familiar with e-source reporting via an electronic platform
• A clear understanding of ICH, FDA, and GCP regulations
• Impeccable organizational skills and attention to detail
• Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
• An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
• High-level critical thinking skills
• Working knowledge of medical terminology and lab collection/processing/storage procedures
• Proficiency with computers and Microsoft Office Suite

Responsibilities

• The Clinical Research Coordinator (CRC) obtains informed consent from the study participants.
• Executes study protocol procedures in a detailed, organized, and professional manner.
• Performs human specimen lab draws and processing, and packages specimen shipments.
• Creates and completes study source documents and adverse event reporting on an e-source system.
• Maintains study-specific files and supplies.
• Communicate with the Study Sponsor/CRO regarding study-specific questions.
• Participates in site visits from Sponsors/CROs, including site initiation and monitoring visits.

Benefits

• Health, dental, and vision insurance plans
• 401(k) with a 100% employer match on the first 4% of employee contributions
• Tuition reimbursement
• Parental leave
• Referral program
• Employee assistance program
• Life insurance
• Disability insurance
• 15 days of PTO + 8 paid holidays and 2 floating holidays.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level