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Clinical Study Coordinator - Phase 1

1-2 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 Study Coordinator - Phase 1

Location: Salt Lake City, UT (100% on-site)

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

Responsibilities:

  • Coordinate and manage the day-to-day conduct of early-phase clinical trials in compliance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements.

  • Support study start-up activities, including IRB submissions, regulatory document collection, and participant screening processes.

  • Act as a liaison between various sponsors, monitors, and internal departments to ensure timely communication and issue resolution.

  • Assist in the preparation and conduct of monitoring visits, audits, and inspections.

  • Collect, review, and ensure the accuracy and completeness of study data and source documentation.

  • Manage subject visits, including scheduling, consent, procedure coordination, and follow-up.

  • Contribute to continuous improvement efforts, including SOP development and workflow optimization.

  • Maintain study documentation in accordance with regulatory and institutional standards.

Qualifications:

  • High school diploma or equivalent (required).

  • Bachelor's degree in a health-related or scientific field (preferred).

  • At least 1–2 years of experience in clinical research or a healthcare setting, ideally within a Clinical Study Coordinator role.

  • Solid understanding of clinical trial processes and GCP requirements.

  • Ability to manage multiple priorities in a fast-paced environment.

  • Excellent attention to detail and strong organizational skills.

  • Effective communication and interpersonal skills, with the ability to work collaboratively in a team-oriented environment.

  • Proficiency with Microsoft Office and familiarity with EDC systems (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.