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Crc Level 2

2+ years
Not Disclosed
10 April 23, 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 (CRC Level 2)

Location: Knoxville, TN (Office-Based)

About ICON plc: ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence.

Responsibilities:

  • Lead the coordination and implementation of clinical trial activities, including patient recruitment, screening, enrollment, and follow-up, ensuring compliance with protocol requirements and regulatory standards.

  • Oversee the maintenance and organization of study documentation and regulatory files, managing study binders, case report forms (CRFs), and electronic data capture (EDC) systems.

  • Collect, record, and enter data into study databases and EDC systems, performing data query resolution and ensuring data accuracy and completeness.

  • Assist with the preparation and submission of regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs).

  • Provide guidance and training to junior staff and study team members on study procedures, protocol requirements, and regulatory compliance.

Qualifications:

  • Bachelor's degree in life sciences, healthcare, or related field; relevant experience may be considered in lieu of a degree.

  • Minimum of 2 years of experience in clinical research or healthcare setting, with demonstrated proficiency in study coordination and data management.

  • Strong organizational skills and attention to detail, with the ability to effectively prioritize and manage multiple tasks and responsibilities.

  • Excellent communication and interpersonal skills, with the ability to interact professionally with study participants, investigators, sponsors, and colleagues.

  • Proficiency in Microsoft Office suite (Word, Excel, Outlook) and experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is preferred.

What ICON can offer you:

  • Competitive salary and a range of benefits focused on well-being and work-life balance.

  • Various annual leave entitlements, health insurance offerings, and retirement planning options.

  • Access to the Global Employee Assistance Programme, LifeWorks, for 24-hour support.

  • Life assurance and flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, and discounted gym memberships.

At ICON, inclusion & belonging are fundamental to our culture and values. We are committed to providing an environment free from discrimination and harassment.