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Clinical Research Associate, Sponsor Dedicated

2+ years
$64,000 – $189,000
10 Nov. 11, 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)

Location: Durham, North Carolina (Field-Based)
Job ID: R1481700
Employment Type: Full-time
Additional Locations: California, Kansas, New Jersey, North Carolina, Remote
Eligibility: Must reside in the same country as the job location


About the Role

This CRA position is ideal for candidates at the beginning or mid-stage of their clinical research career. The role provides strong training, mentorship, and quarterly structured performance reviews for career development.
You will work on global projects using advanced in-house technology, with travel limited to your region/home state.


Key Responsibilities

Site Management

  • Conduct site selection, initiation, monitoring, and close-out visits.

  • Maintain all required study documentation.

Study Support

  • Assist in developing subject recruitment plans.

  • Provide protocol and study-related training to assigned sites.

  • Maintain regular communication with site staff.

Quality & Compliance

  • Evaluate site practices for quality and protocol integrity.

  • Escalate quality issues when necessary.

  • Track regulatory submissions, recruitment status, CRF completion, and data queries.


Required Qualifications

  • Bachelor's degree in a healthcare or scientific discipline (or equivalent).

  • Completion of a CRA Trainee Program or minimum 3 months on-site monitoring experience.

  • 2 years of Clinical Research Coordinator experience strongly preferred.

  • Equivalent combinations of education, training, and experience will be considered.

  • Basic knowledge of clinical research regulatory requirements.


Why Join IQVIA?

  • Access to innovative technology and global projects.

  • Strong career development pathways.

  • Flexible, region-based travel.

  • Work that makes a global impact on patient health.


Compensation & Benefits

  • Base Salary Range: $64,000 – $189,000 (annualized).

  • Final offer varies based on skills, experience, education, and location.

  • May include incentive plans, bonuses, and comprehensive benefits.


About IQVIA

A leading global provider of clinical research, healthcare intelligence, and commercial insights. IQVIA accelerates medical innovation to improve patient outcomes worldwide.