CRA 2/Senior CRA 1

QHR IQVIA Zagreb d.o.o.

Apply to this job
Durham, North Carolina, US Columbia, Maryland, US Until 8/21/2026 1+ years exp First posted June 2, 2026 Last posted June 2, 2026
Job description

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.
About this role

Summary

Conduct site monitoring, ensure compliance, and manage clinical study progress.

Job title

CRA 2/Senior CRA 1

Experience level

1.5+ years

Minimum experience

1+ years exp

Industry

healthcare

Location requirements

Multiple US locations, remote work not specified.

Salary

$90k–$175k

Management role

No

Skills & keywords

Required skills

GCPICHregulatory requirementscommunicationorganization

Preferred skills

None specified

Specializations

clinical trialsmonitoringregulatory complianceGCPICH
Locations

Structured locations inferred from the posting.

Durham, NC, USA

Work arrangement unknown City

Columbia, MD, USA

Work arrangement unknown City

Phoenix, AZ, USA

Work arrangement unknown City

Gilbert, AZ, USA

Work arrangement unknown City

San Francisco, CA, USA

Work arrangement unknown City

Annapolis, MD, USA

Work arrangement unknown City

Chicago, IL, USA

Work arrangement unknown City

Glendale, AZ, USA

Work arrangement unknown City

New York, NY, USA

Work arrangement unknown City

Sacramento, CA, USA

Work arrangement unknown City

Houston, TX, USA

Work arrangement unknown City

Indianapolis, IN, USA

Work arrangement unknown City

Rockville, MD, USA

Work arrangement unknown City

Carlsbad, CA, USA

Work arrangement unknown City

Dallas, TX, USA

Work arrangement unknown City