Instagram
youtube
Facebook

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 – Raleigh, NC (On-Site)

Job Summary:

ICON plc, a global leader in healthcare intelligence and clinical research, is hiring a Clinical Research Coordinator (CRC Level I) in Raleigh, North Carolina. This full-time, on-site role is perfect for candidates passionate about clinical development, patient safety, and operational excellence. You’ll support trial execution by managing clinical procedures, patient engagement, regulatory compliance, and sponsor communications. Ideal for life science graduates or professionals with early experience in clinical trials, this is a gateway to long-term growth in clinical research.


Key Responsibilities:

  • Perform clinical procedures per study protocols: venipuncture, ECGs, IV infusions, injections, specimen collection.

  • Attend site initiation, investigator, and coordinator meetings.

  • Maintain dispensing logs and monitor for complications during drug administration.

  • Document lab data, adverse events, and ensure prompt reporting to investigators and IRBs.

  • Recruit suitable participants and promote clinical trials effectively.

  • Prepare for sponsor/FDA audits and maintain regulatory documentation.

  • Manage investigational product storage, temperature monitoring, and equipment calibration.

  • Order clinical supplies, oversee crash cart and AED checks.

  • Support team development and train site staff as needed.


Required Skills & Qualifications:

  • Bachelor's degree in life sciences or related field preferred.

  • At least 1 year of experience in clinical research or pharma industry (preferred).

  • Familiarity with GCP, FDA, IRB processes.

  • Excellent attention to detail and planning skills.

  • Personable, motivated, and patient-focused.

  • Comfortable with data entry, lab documentation, and protocol compliance.


Perks & Benefits:

  • Competitive salary (specific compensation not disclosed).

  • Annual leave entitlements.

  • Comprehensive health insurance packages.

  • Retirement savings plans.

  • Global Employee Assistance Programme.

  • Life assurance.

  • Country-specific benefits: travel passes, gym discounts, childcare vouchers, and more.

  • Inclusive and supportive work culture.


Company Description:

ICON plc is a global clinical research organization providing outsourced development and commercialisation services to pharmaceutical, biotechnology, and medical device industries. With a commitment to excellence, ICON helps accelerate the development of drugs and devices that save lives and improve quality of care worldwide.


Work Mode:

On-Site – Raleigh, NC


Call-to-Action:

Join ICON and take your clinical research career to the next level. Apply now to be part of a global healthcare team driving innovation in drug development and patient care.