Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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.