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Partner with investigative sites and cross-functional teams to ensure clinical trials are executed with excellence, compliance, and patient focus.

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

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

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

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.
We create connections that accelerate the development and commercialization of innovative medical treatments.
Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact.
No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

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.
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.

CRA 2/Senior CRA 1 at IQVIA

CRA 2/Senior CRA 1