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About the Role

We are seeking a passionate and driven Clinical Research Associate (CRA) with 1-3 years of on-site monitoring experience to join our FSP Sponsor Dedicated team. You will play a key role in delivering high-quality clinical trials by partnering with investigative sites and cross-functional teams to ensure excellence, compliance, and patient focus.

Responsibilities

• 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

Requirements

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

Location

• Regional

Work Type

• On-site monitoring

Experience Level

• 1-3 years of on-site monitoring experience

Education Level

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

Salary/Compensations

• $90,200.00 - $175,100.00

Benefits

• Opportunities for growth and career development
• Incentive plans, bonuses, and/or other forms of compensation may be offered
• Range of health and welfare and/or other benefits

About the Company

• 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

Equal Opportunity

• 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.