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Clinical Research Coordinator 2

3+ years
Not Disclosed
10 April 24, 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

Job Title: Clinical Research Coordinator 2

Location: Knoxville, TN (100% On-Site)

About ICON plc:
ICON plc is a global healthcare intelligence and clinical research organization. We are committed to delivering excellence by fostering a diverse and inclusive workplace that champions innovation, collaboration, and career growth.

Role Summary:
We are seeking a Clinical Research Coordinator 2 (CRC 2) to join our Accellacare/ICON team in Knoxville, TN. This is a fully on-site position where you will coordinate and manage the day-to-day activities of clinical trials to ensure successful execution, regulatory compliance, and high-quality data collection.

Responsibilities:

  • Coordinate the operational aspects of clinical trials, including participant recruitment, visit scheduling, and site logistics.

  • Ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

  • Monitor and document study progress, including safety reporting and adherence to timelines.

  • Provide training and support to site staff to ensure proper execution of trial procedures.

  • Build and maintain positive relationships with study participants and site personnel.

  • Collaborate with cross-functional teams to resolve issues and ensure efficient trial operations.

Qualifications:

  • Bachelor’s degree in Life Sciences, Healthcare Management, or a related field.

  • Minimum of 3 years’ experience as a Clinical Research Coordinator.

  • Thorough knowledge of clinical trial operations and regulatory standards.

  • Proficiency in clinical trial software and strong documentation skills.

  • Strong organizational and multitasking abilities with attention to detail.

  • Excellent interpersonal, communication, and problem-solving skills.

What ICON Can Offer You:

  • Competitive salary with performance-based incentives.

  • Various annual leave entitlements tailored to local market.

  • A wide range of health insurance plans to support you and your family.

  • Retirement planning options to help secure your financial future.

  • Access to LifeWorks – Global Employee Assistance Programme for mental and emotional support.

  • Life assurance and other flexible, region-specific benefits including:

    • Childcare vouchers

    • Bike-to-work schemes

    • Gym membership discounts

    • Subsidized travel passes

    • Preventative health assessments

ICON is committed to equality, diversity, and inclusion. We encourage all qualified individuals to apply and provide reasonable accommodations during the hiring process upon request.