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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 – Mt Pleasant, SC

Job Summary:
ICON plc, a global leader in clinical research and healthcare intelligence, is hiring a Clinical Research Coordinator (CRC Level I) in Mt Pleasant, SC. This on-site role offers an exciting opportunity to work with Accellacare, ensuring volunteer safety and study compliance while building a career in the clinical research industry. Ideal for candidates with at least 1 year of relevant experience in clinical trials or the pharmaceutical sector.


Key Responsibilities:

  • Conduct technical and clinical study procedures (e.g., venipuncture, ECGs, IV infusions, pulmonary function testing).

  • Attend site initiation and investigator meetings for protocol training.

  • Monitor and manage investigational drug administration and related complications.

  • Maintain accurate study and dispensing logs.

  • Document adverse reactions, lab data, and report serious events promptly.

  • Participate in patient recruitment and trial promotion.

  • Prepare study documentation for audits and inspections.

  • Monitor clinical supply inventory and manage crash cart protocols.

  • Calibrate and maintain equipment and lab devices.

  • Support clinical skill training for site staff.


Required Skills & Qualifications:

  • Bachelor’s degree in Life Sciences or related field

  • Minimum 1 year of experience in clinical research or pharmaceutical environment

  • Hands-on clinical skills (e.g., venipuncture, ECGs, injections)

  • Knowledge of GCP, FDA regulations, and clinical trial processes

  • Strong attention to detail and organizational skills

  • Excellent communication and patient interaction skills

  • Motivated and passionate about clinical research


Perks & Benefits:

  • Competitive salary

  • Comprehensive health insurance options

  • Generous paid leave entitlements

  • Retirement planning programs

  • Global Employee Assistance Program (EAP)

  • Life assurance and optional country-specific benefits

  • Career development and training support

  • Inclusive, diverse work environment


Company Description:

ICON plc is a world-renowned clinical research organization specializing in healthcare intelligence and development solutions. With a presence in over 40 countries, ICON provides industry-leading services to pharmaceutical, biotech, and medical device companies, delivering innovations that advance global health.


Work Mode:
On-Site – Mt Pleasant/Charleston, SC


Call-to-Action:
Ready to take the next step in your clinical research career? Apply now to join ICON plc as a Clinical Research Coordinator in Mt Pleasant and be part of a team shaping the future of clinical development.