Clinical Research Coordinator
Charlotte
Clinical Research Coordinator
Full Time • Charlotte
Benefits:
- Company parties
- Competitive salary
- Health insurance
- Opportunity for advancement
- Paid time off
- Training & development
Position: Clinical Research Coordinator (Experienced)
Location: Charlotte, NC
Schedule: Full‑time, on‑site
Education Requirement: Associate’s degree or nursing certificate
Experience Requirement: Minimum 1+ year of hands‑on CRC experience
Schedule: Full‑time, on‑site
Education Requirement: Associate’s degree or nursing certificate
Experience Requirement: Minimum 1+ year of hands‑on CRC experience
About the Role
We are seeking an Experienced Clinical Research Coordinator to support the conduct of clinical trials across multiple therapeutic areas. The ideal candidate is detail‑oriented, proactive, and comfortable managing study visits independently while maintaining exceptional participant care and regulatory compliance.
Key Responsibilities
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Study Coordination — Manage day‑to‑day study operations, ensuring strict adherence to protocol, GCP, and site SOPs.
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Participant Management — Recruit, screen, consent, and schedule participants; conduct study visits and assessments.
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Informed Consent — Lead the consent process with clarity, accuracy, and ethical compliance.
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Source Documentation — Maintain complete, audit‑ready source documents and reconcile with EDC entries.
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Data Entry & Query Resolution — Enter high‑quality data, resolve queries promptly, and meet sponsor deadlines.
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Regulatory Support — Assist with IRB submissions, essential documents, delegation logs, and training records.
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Specimen Processing — Process, label, centrifuge, freeze, and ship biological samples per protocol.
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Safety Reporting — Document and report AEs/SAEs; collaborate with investigators on assessments.
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Monitor & Sponsor Interaction — Prepare for monitoring visits, respond to findings, and maintain professional communication.
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Study Supplies — Track inventory, maintain equipment logs, and ensure visit readiness.
Required Qualifications
- Associate’s degree in a health‑related field or nursing certificate/degree (LPN, RN, BSN with clinical experience)
- Minimum 1+ year of experience as a Clinical Research Coordinator
- Proficiency with EDC systems (Rave, Inform) and Microsoft Office
- Ability to perform vitals, ECGs, phlebotomy, and sample processing
- Strong understanding of GCP, ICH, FDA regulations, and IRB processes
- Excellent communication, organization, and time‑management skills
Preferred Qualifications
- Experience in oncology, immunology, cardiology, or CNS
- Familiarity with PK/PD sampling or complex visit schedules
- Experience with eReg systems (Veeva)
- Bilingual skills
What We Offer
- Competitive compensation
- Opportunities for professional development and advancement
- Supportive team environment
- Exposure to diverse therapeutic areas and study types
Compensation: $20.00 - $25.00 per hour
ABOUT
At Joint Muscle Medical Care and Research Institute, we are focused on exceeding expectations by delivering the best care with the highest levels of customer satisfaction to each one of our patients.
Why Us
We are a privately own Rheumatology practice that is interested in putting our patient care first and we are driven by innovative care in preventing advancement of inflammatory conditions like Rheumatoid Arthritis, Systemic Lupus Erythematosus, Psoriatic Arthritis, Gout, and other immunological driven diseases.
We are recognized as Thought Leaders by our peers and are active participants in latest Clinical Research Trials with prestigious pharmaceutical companies.
Our team is solidified around two board certified Rheumatologists that are FACR (Fellows of American College of Rheumatology) and active members of EULAR (European League Against Rheumatism).
We are recognized as Thought Leaders by our peers and are active participants in latest Clinical Research Trials with prestigious pharmaceutical companies.
Our team is solidified around two board certified Rheumatologists that are FACR (Fellows of American College of Rheumatology) and active members of EULAR (European League Against Rheumatism).
Our mission is
- to improve Quality of Life and stop the progression of debilitating diseases using targeted treatment choices while providing compassionate care.
- to empower patients to become active participants in their care.
- to become a patient advocate and strive to provide care that not only is effective but also safe.
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