CRA 2/Senior CRA 1

15 LOCATIONS (OTHER)HYBRIDPOSTED: 6/24/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
Iqvia

ROLE DEFINITION & RESPONSIBILITIES

Join a Team That’s Advancing Clinical Research We’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 Do 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

What You Bring Bachelor’s degree in life sciences, healthcare, or related field (or equivalent experience)

1.5+ years of on-site monitoring experience

Solid understanding of GCP, ICH, and regulatory requirements

Strong communication, problem-solving, and organizational skills

Ability to manage multiple priorities in a fast-paced environment

Why Join Us Make a direct impact on advancing clinical research and improving patient outcomes

Work alongside experienced, collaborative teams

Opportunities for growth and career development

Dynamic, 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.com

IQVIA 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/eoe

IQVIA 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 $90,200.00 - $175,100.00. 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.

REQUIRED VERIFIED SKILLS

GCP
Clinical Trials
Clinical Research
Excel

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Salary for this CRA 2/Senior CRA 1 position is competitive and aligned with industry standards for this location.

ORGANIZATION CONTEXT & CULTURE

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.

TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research

EXPECTED CAREER ROADMAP

Regulatory Affairs Executive ➔ Senior RA Specialist ➔ Regulatory Affairs Manager ➔ Director.

APPLICATION ADVISORY

Ensure your resume clearly showcases experience with: GCP, Clinical Trials, Clinical Research. Prepare real-world examples demonstrating these skills for the interview.
RECOMMENDED TRAINING
1/5

READY TO SUBMIT?

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