Clinical Research Coordinator

Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. We embrace employees, customers, and patients from underrepresented groups to help make excellence in clinical trials and healthcare a reality for everyone.

About the role

We are actively hiring a Clinical Research Coordinator to support our Inverness, FL site. This is an onsite, non-exempt position with normal work hours Monday through Friday.

Responsibilities

• Execute protocol-specified patient visits and procedures, which may include phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.
• Document assessments and study data per regulations and Good Clinical Practice (GCP); maintain complete source; accurately complete CRFs/eCRFs.
• Obtain informed consent per federal regulations, GCP, and IRB requirements.
• Ethically recruit qualified subjects to meet enrollment timelines.
• Complete required and ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies.
• Schedule and conduct visits per protocol timelines.
• Protect confidentiality per HIPAA and all confidentiality agreements.
• Report adverse events (AEs) promptly; report serious adverse events (SAEs) to sponsor within 24 hours and notify 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- and cost-effective manner compliant with Flourish policies.
• Represent Flourish professionally in all interactions.
• Additional duties as assigned by management.

Requirements

• Bachelor's degree preferred, but not required.
• Minimum of two years of clinical research experience.
• Oncology clinical research experience required.
• Clinical skills highly 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 honesty, detail-orientation, and self-drive.
• High-level critical thinking skills.
• Working knowledge of medical terminology and lab collection/processing/storage procedures.
• Proficiency with computers and Microsoft Office Suite.

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.
• Employee referral program.
• Employee assistance program.
• Life insurance and disability insurance.
• Generous PTO plan covering vacation, sick, personal days, and 8 paid holidays.