Clinical Research Coordinator, On-Site, Springville, Utah

2+ years

Not Disclosed

Springville

10 Aug. 29, 2025

Job Description

Job Type: Full Time Education: rior experience as a Clinical Research Coordinator 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

Location: Springville, Utah
Job Type: Full-Time
Work Set-Up: Fully On-Site (Office-based)
Job ID: R1489894
Availability: Position also available in additional locations
Company: IQVIA / Avacare Clinical Research

Position Overview:

Join a collaborative, patient-focused team supporting groundbreaking clinical studies. This Clinical Research Coordinator (CRC) role offers the opportunity to grow your clinical research expertise in a fast-paced, supportive environment where professional development is valued. Ideal for individuals who are detail-oriented, team-driven, and passionate about improving patient outcomes through research.

Key Responsibilities:

Clinical Study Coordination

Coordinate and conduct clinical research studies under the supervision of a Principal Investigator.
Assist as back-up CRC on other ongoing studies as needed.
Develop and execute patient recruitment strategies to meet enrollment targets.
Schedule research participants for study-related visits and procedures.
Obtain informed consent from research participants in compliance with ethical and regulatory standards.

Data & Documentation

Collect and maintain patient history and source documentation.
Perform data entry and resolve queries accurately and in a timely manner.
Manage investigational products, administer test articles, and maintain inventory.
Support collection and review of essential study documents and reports.
Order and track study-related materials and supplies (e.g., lab kits, manuals, contracts).

Protocol Compliance & Participant Safety

Adhere strictly to IRB-approved study protocols.
Ensure compliance with GCP/ICH and all applicable regulatory guidelines.
Report adverse events and assist with safety monitoring of participants.
Coordinate protocol-related procedures, study visits, and follow-ups.

Site Management

Support pre-study, site qualification, initiation, monitoring, and close-out visits.
Collect, process, and ship lab specimens per protocol.
Participate in special projects and travel to nearby clinic locations if required.
Comply with IQVIA/Avacare and sponsor SOPs, policies, and procedures.
Perform additional duties as assigned.

Qualifications:

Experience:
- Prior experience as a Clinical Research Coordinator required.
- Familiarity with clinical site operations and the drug development process.
Clinical Skills:
- Experience with vital signs, phlebotomy, EKG, and other clinical procedures.
Knowledge & Compliance:
- Strong understanding of GCP, ICH, and regulatory requirements.
- Ability to adhere to protocol, SOPs, and ethical standards.
Technical Skills:
- Proficiency with Microsoft Word and Excel.
- Effective verbal and written communication skills.

Compensation & Benefits:

Base Pay Range (Annualized): $36,600.00 – $91,300.00
(Final offer based on experience, skills, education, location, and work schedule.)
Additional compensation may include incentive plans, bonuses, and a full range of health and welfare benefits.

About IQVIA:

IQVIA is a global leader in clinical research, healthcare intelligence, and data-driven solutions for the life sciences industry. We are committed to accelerating medical innovation and improving health outcomes.
Learn more: https://jobs.iqvia.com

Equal Opportunity Employer:

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected characteristics.
EEO Policy: https://jobs.iqvia.com/eoe

How to Apply:

Visit https://jobs.iqvia.com and search for Job ID R1489894, or click Apply Now.

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Clinical Research Coordinator, On-Site, Springville, Utah

Job Description

Job Title: Clinical Research Coordinator

Position Overview:

Key Responsibilities:

Clinical Study Coordination

Data & Documentation

Protocol Compliance & Participant Safety

Site Management

Qualifications:

Compensation & Benefits:

About IQVIA:

Equal Opportunity Employer:

How to Apply:

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