Exciting opportunity at ICON plc – a global leader in clinical research! Join as Clinical Research Coordinator Level 2 in Knoxville, Tennessee. 2+ years CRC experience required. Transform clinical trials with Accellacare. Apply now for clinical research jobs in USA!
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About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to accelerating the development of life-changing therapies. With a global footprint and over 40,000 employees, ICON partners with pharmaceutical, biotechnology, and medical device companies to deliver innovative clinical research solutions.
Through its Accellacare site network, ICON enhances patient access, improves trial efficiency, and drives better outcomes. Recognized for fostering an inclusive culture, ICON prioritizes diversity, innovation, employee well-being, and excellence in clinical development.
Job Details
- Company Name: ICON plc (Accellacare Network)
- Position: Clinical Research Coordinator – Level 2 (JR134248)
- Experience: Minimum 2+ years as patient-facing Clinical Research Coordinator
- Qualification: Bachelor’s degree in Life Sciences or related field
- Location: Knoxville, Tennessee, USA (1200 Merchant Drive, Knoxville, TN 37912)
- Work Type: On-site (Office Based)
Job Description
ICON’s Accellacare team is actively seeking an experienced Clinical Research Coordinator Level 2 to support multiple clinical trials at its Knoxville site. This pivotal onsite role focuses on patient safety, study execution excellence, recruitment success, and site quality while mentoring junior staff.
You will work autonomously on complex protocols, build strong investigator relationships, and contribute directly to advancing global clinical research.
Clinical Research Coordinator – Level 2
- Department: Clinical Research Site Services
- Role: CRC Level 2 (Mentoring & Autonomous Study Coordination)
- Experience: 2+ years patient-facing CRC experience required
- Education/Qualification: Bachelor’s degree in Life Sciences or healthcare-related field
- Location: Onsite – Knoxville, TN
Skills/Qualifications
- Minimum 2 years of direct patient-facing CRC experience
- Bachelor’s degree in Life Sciences or equivalent
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements
- Proficiency in CTMS, EDC systems, and CRF completion
- Excellent recruitment and patient screening abilities
- Phlebotomy and clinical skills (ECG, vital signs, lab processing)
- Superior organizational and time-management skills
- Strong communication and relationship-building capabilities
- Motivated, detail-oriented, and quality-focused mindset
Key Responsibilities
- Develop and execute effective recruitment plans
- Screen and enroll participants per protocol
- Perform study start-up and site initiation activities
- Collect accurate study data via source documents
- Conduct phlebotomy, ECGs, vital signs, and protocol procedures
- Dispense investigational product under investigator direction
- Enter data into EDC/CRF within sponsor timelines
- Report adverse events and protocol deviations promptly
- Attend investigator meetings and monitor visits
- Mentor junior CRCs and support site quality assurance
Benefits/Perks
- Competitive salary package
- Comprehensive health insurance options
- Generous annual leave entitlements
- Robust retirement savings plans
- Global Employee Assistance Programme (24/7 support)
- Life assurance coverage
- Flexible country-specific benefits (gym, childcare, transport)
- Career development and training opportunities
- Inclusive and supportive global culture
How to Apply
Apply directly through the official ICON careers portal: Search for JR134248 – Clinical Research Coordinator 2, Knoxville
For more clinical research jobs in the USA and globally, visit Pharma Recruiter.
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Even if you’re unsure about meeting every requirement — ICON encourages you to apply!
Why You Should Join
At ICON, you’ll be part of a mission-driven organization that shapes the future of clinical development. Working within the Accellacare network means delivering faster, more efficient trials that bring new treatments to patients sooner.
With a strong emphasis on inclusion, professional growth, work-life balance, and recognition, ICON offers long-term career stability and the chance to make a real impact in healthcare.
FAQs
Is prior CRC experience mandatory?
Yes, at least 2 years of patient-facing Clinical Research Coordinator experience is required.
Is this a remote or hybrid role?
No, this is a fully onsite position based in Knoxville, TN.
What clinical skills are needed?
Phlebotomy, ECG, vital signs, lab processing, and other protocol-specific procedures are essential.
Does ICON offer relocation assistance?
Benefits and relocation support are discussed with shortlisted candidates. ICON provides competitive packages tailored to top talent.