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Clinical Research Associate, Sponsor Dedicated

0-2 years
$64,000.00 - $189,000.00
10 Nov. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

 

Clinical Research Associate (Sponsor-Dedicated) | IQVIA

Location: Durham, North Carolina
Job Type: Full-Time
Job ID: R1481700
Work Model: Field-Based
Additional Locations Available Across the United States

Role Overview

IQVIA is seeking a Sponsor-Dedicated Clinical Research Associate (CRA) to support high-quality clinical trial execution across regional sites. This position offers a strong foundation for individuals beginning or advancing their CRA career. Candidates must be residents of the country where the role is based.

This opportunity includes structured professional development, dedicated mentoring, quarterly performance reviews, and access to advanced in-house technologies. You will contribute to global clinical research while maintaining a regional or home-state travel scope, enabling a flexible and sustainable career path.


Key Responsibilities

  • Conduct site selection, initiation, routine monitoring, and close-out visits while maintaining precise documentation in accordance with study requirements.

  • Support the development and execution of subject recruitment strategies to meet enrollment timelines.

  • Establish consistent communication with investigative sites and deliver protocol-specific and study-related training.

  • Evaluate site performance, ensuring adherence to protocol, regulatory guidelines, and data quality standards, and escalate issues appropriately.

  • Track study progress including regulatory submissions, patient recruitment, CRF completion, and data query resolution.

  • Collaborate effectively with internal stakeholders, site staff, and sponsor teams to support successful trial delivery.


Required Qualifications

  • Bachelor’s degree in a healthcare, life sciences, or scientifically relevant field (or equivalent education and training).

  • Successful completion of a recognized CRA Trainee Program or a minimum of three months of on-site monitoring experience.

  • Two years of Clinical Research Coordinator (CRC) experience strongly preferred.

  • Alternatively, an equivalent combination of education, training, and relevant industry experience may be considered.

  • Fundamental understanding of clinical research regulations, including ICH GCP, and comfort working with cross-functional teams.


Why Join IQVIA

IQVIA is a global leader in healthcare intelligence, clinical research, and advanced analytics. The company partners with leading life sciences organizations to accelerate medical innovation and improve patient outcomes worldwide.

IQVIA is committed to fostering an inclusive and diverse workplace and welcomes applicants from all backgrounds.


Compensation

Annual Base Pay Range:
$64,000 – $189,000

Actual compensation may vary based on qualifications, experience, geographic location, and work schedule. Additional benefits, incentive programs, and performance-based bonuses may be offered depending on the role.