CRA 2/Senior CRA - FSP Sponsor Dedicated

About the role

We’re looking for a passionate and driven Clinical Research Associate (CRA) with 1-3 years of on-site monitoring experience to join our FSP Sponsor Dedicated team and play a key role in delivering high-quality clinical trials.

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
• Able to manage multiple priorities in a fast-paced environment

Qualifications

• Experience in clinical research or related field
• Knowledge of Good Clinical Practices (GCP) and International Conference on Harmonisation (ICH) guidelines
• Excellent interpersonal and communication skills
• Ability to work independently and as part of a team

Skills

• Strong analytical and problem-solving skills
• Effective time management and organization skills
• Proficiency in Microsoft Office Suite
• Ability to travel up to 65-70% of the time

Benefits

• Comprehensive health and welfare benefits
• Professional development opportunities
• Flexible work arrangements
• Work-life balance initiatives

Pay

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).

Schedule

Full-time position with regional travel required.

Contact

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. Learn more about our commitment to diversity and inclusion.

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.