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Clinical Research Coordinator

1+ years
Not Disclosed
10 July 21, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Clinical Research Coordinator – Wilmington, NC (On-site)

Job Summary:
ICON plc, a global leader in clinical research and healthcare intelligence, is hiring a Clinical Research Coordinator (CRC Level I) in Wilmington, NC. This on-site role supports end-to-end clinical trial coordination, ensuring participant safety and protocol compliance. Ideal for life sciences graduates with clinical research or pharmaceutical exposure, this position offers hands-on involvement in clinical operations, technical procedures, and patient recruitment.


Key Responsibilities:

  • Perform protocol-based clinical procedures (e.g., venipuncture, ECGs, IV infusions, allergy testing, pregnancy/strep tests).

  • Attend study meetings to understand drug administration protocols.

  • Handle and document investigational products, including preparation and dispensing logs.

  • Monitor for and report adverse events, liaising with investigators and sponsors.

  • Recruit and screen trial participants; actively promote the site to sponsors.

  • Maintain study documentation for audits and regulatory compliance.

  • Manage clinical supplies and emergency drug inventory (rescue medications, crash carts).

  • Calibrate and maintain clinical equipment and temperature-monitoring devices.

  • Act as OSHA Representative (e.g., employee immunizations, vaccine administration).

  • Support site staff with training in clinical procedures.


Required Skills & Qualifications:

  • Bachelor’s degree in Life Sciences or equivalent relevant experience.

  • Minimum 1 year of clinical research or pharmaceutical industry experience (preferred).

  • Familiarity with clinical protocols, regulatory documentation, and GCP.

  • Proficient in phlebotomy, vital signs, ECG, and lab procedures.

  • Strong organizational and planning skills.

  • Comfortable interacting with patients and promoting clinical trials.

  • Proactive attitude with attention to detail and data accuracy.


Perks & Benefits:

  • Competitive salary (range not specified, but industry-aligned)

  • Generous annual leave

  • Health insurance plans tailored to employee and family needs

  • Retirement planning options

  • Life assurance

  • Global Employee Assistance Program (LifeWorks)

  • Optional country-specific perks (e.g., gym discounts, childcare vouchers, health assessments)


Company Description:

ICON plc is a world-renowned healthcare intelligence and clinical research organization. With a focus on innovation, compliance, and patient-centered research, ICON partners with top pharmaceutical, biotech, and medical device companies to drive advancements in global health outcomes.


Work Mode: On-site (Wilmington, NC)


Call to Action:

If you are motivated to build a career in clinical research and meet the required skills, apply today to join ICON plc. Shape the future of drug development with a global leader in clinical trials.