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CRA 2/Senior CRA

IQVIA

CRA 2/Senior CRA

full-timePosted: Aug 2, 2026Updated: Sep 1, 2026United States of America, North Carolina, Durham

Job Description

Join a Team That’s Advancing Clinical ResearchWe’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.What You’ll DoLead and execute site monitoring visits (selection, initiation, routine, and close-out) in accordance with GCP/ICH guidelinesBuild strong relationships with investigative sites to drive performance, recruitment, and engagementEnsure protocol compliance, data integrity, and high-quality study executionProactively identify risks, resolve issues, and escalate when neededTrack and manage study progress, including regulatory approvals, enrollment, and data qualityMaintain accurate documentation and contribute to inspection readinessCollaborate with cross-functional teams to ensure successful study deliveryWhat You BringBachelor’s degree in life sciences, healthcare, or related field (or equivalent experience)1+ year of on-site monitoring experienceSolid understanding of GCP, ICH, and regulatory requirementsStrong communication, problem-solving, and organizational skillsAbility to manage multiple priorities in a fast-paced environmentWhy Join UsMake a direct impact on advancing clinical research and improving patient outcomesWork alongside experienced, collaborative teamsOpportunities for growth and career developmentDynamic, fast-paced environment where your contributions matter👉 If you’re ready to take the next step in your CRA career and be part of meaningful, impactful work, we’d love to hear from you.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $87,200.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Locations

  • United States of America, North Carolina, Durham
  • United States of America, AZ, Gilbert
  • United States of America, AZ, Phoenix
  • United States of America, CA, San Francisco
  • NY United States of America, New York
  • United States of America, Indiana, Indianapolis
  • United States of America, CA, Sacramento
  • United States of America, AZ, Scottsdale
  • United States of America, Illinois, Chicago
  • United States of America, CA, Carlsbad
  • United States of America, Texas, Dallas
  • United States of America, TX, Houston

Required Qualifications

  • Bachelor’s degree in life sciences, healthcare, or related field (or equivalent experience) (experience)
  • 1+ year of on-site monitoring experience (experience, 1 years)
  • Solid understanding of GCP, ICH, and regulatory requirements (experience)
  • Strong communication, problem-solving, and organizational skills (experience)
  • Ability to manage multiple priorities in a fast-paced environment (experience)

Responsibilities

  • Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in accordance with GCP/ICH guidelines
  • Build strong relationships with investigative sites to drive performance, recruitment, and engagement
  • Ensure protocol compliance, data integrity, and high-quality study execution
  • Proactively identify risks, resolve issues, and escalate when needed
  • Track and manage study progress, including regulatory approvals, enrollment, and data quality
  • Maintain accurate documentation and contribute to inspection readiness
  • Collaborate with cross-functional teams to ensure successful study delivery

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