Iqvia
(Senior) Clinical Research Associate
Durham, North Carolina, United States of America · Overland Park, KS, United States of America · Parsippany, New Jersey, United States of America · Carlsbad, CA, United States of America
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.
Tailor my resume for this job →hirly's read of this role
- Role family
- Healthcare
- Seniority
- Senior
- Stated salary
- $90,200 per year
- Country
- US
- Work mode
- On-site / unstated
- First seen by hirly
- 1 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
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
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.
Similar jobs
- Senior Clinical Research Associate - Alzheimer's DiseasePropharmagroup · United StatesFirst seen today
- Senior Clinical Research Associate - Contract PositionProtrials · RegionalFirst seen todayremote
- Senior Clinical Research AssociateProtrials · RegionalFirst seen todayremote
- Clinical Research Associate (I, II, III)Teamargenta · Shawnee, Kansas, RemoteFirst seen todayremote
- Clinical Research Associate (CRA II/Senior) - Hematology - US Any RegionParexel · United States - RemoteFirst seen todayremote
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job