Clinical Research Coordinator

Flourish Research•Charlotte, NC

10d•Onsite

About The Position

Flourish Research is hiring a Clinical Research Coordinator to support its Charlotte site. The position performs protocol-driven clinical research visits and procedures, obtains informed consent, recruits participants, documents study data, and supports regulatory compliance and trial operations. Work is onsite in Charlotte, North Carolina, Monday through Friday during regular day-shift hours. A bachelor’s degree is preferred but not required. Candidates must have oncology clinical research experience and at least two years of clinical research experience.

Requirements

Must have oncology clinical research experience.
Minimum of two years of clinical research experience.
Familiarity with e-source reporting via an electronic platform.
Clear understanding of ICH, FDA, and GCP regulations.
Impeccable organizational skills and attention to detail.
Excellent communication and interpersonal skills for interacting with the Principal Investigator, research team, study sponsors/CROs, potential subjects, and referral sources.
Ethical, honest, detail-oriented, and self-driven approach to work.
High-level critical-thinking skills.
Working knowledge of medical terminology and lab collection, processing, and storage procedures.
Proficiency with computers and Microsoft Office Suite.

Nice To Haves

Bachelor’s degree preferred but not required.
Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, and injections.

Responsibilities

Execute protocol-specified patient visits and procedures, which may include phlebotomy, IVs, injections, vital signs, and ECG/EKGs.
Document assessments and study data in accordance with regulations and GCP; maintain complete source documentation and accurately complete CRFs/eCRFs.
Obtain informed consent in accordance with federal regulations, GCP, and IRB requirements.
Ethically recruit qualified subjects to meet enrollment timelines.
Complete required and ongoing training, attend investigator meetings and courses, and stay current with changing regulations and Flourish policies.
Schedule and conduct visits according to protocol timelines.
Protect confidentiality in accordance with HIPAA and confidentiality agreements.
Report adverse events promptly; report serious adverse events to the sponsor within 24 hours and notify the PI, Sub-I, or supervisor.
Account for and ensure availability of trial materials, including study drug, labs, CRFs, and supplies.
Maintain and document communication with Leads, Managers, PIs/Sub-Is, and the study team according to protocol and policy.
Perform duties safely and in a time- and cost-effective manner while complying with Flourish policies.
Represent Flourish professionally in all interactions.
Perform additional duties as assigned by management.