CRA 2Senior CRA 1

Were looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical this role youll partner with investigative sites and cross-functional teams to ensure studies 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

• Bachelors 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

• 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 youre ready to take the next step in your CRA career and be part of meaningful impactful work wed 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

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. 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.