Clinical Research Coordinator

Flourish Research•Boca Raton, FL

28d•Onsite

About The Position

Flourish Research is seeking a motivated and talented Clinical Research Coordinator to support our Boca Raton, Florida site. This is a full-time, 40-hour per week, day shift position. Flourish Research is a progressive clinical trial organization with strong capabilities across various research areas, committed to providing excellent care and fostering a diverse and inclusive work environment. We offer a comprehensive benefits package, a supportive work environment, and growth opportunities.

Requirements

Minimum of two years of clinical research experience
Clinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injections
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

Nice To Haves

Bachelor's degree preferred, but not required

Responsibilities

Execute protocol-specified patient visits and procedures, including phlebotomy, IVs, injections, vital signs, and ECG/EKG.
Document assessments and study data per regulations/GCP, maintain complete source documentation, and accurately complete CRFs/eCRFs.
Obtain informed consent per federal regulations, GCP, and IRB requirements.
Recruit qualified subjects ethically to meet enrollment timelines.
Complete required training, attend investigator meetings/courses, and stay current with regulations and company policies.
Schedule and conduct visits per protocol timelines.
Protect confidentiality per HIPAA and all confidentiality agreements.
Report AEs promptly and SAEs to the sponsor within 24 hours, notifying PI/Sub-I/supervisor.
Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies).
Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy.
Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies.
Represent Flourish professionally in all interactions.
Perform additional duties as assigned by management.