CRA 2/Senior CRA

About the role

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in oncology. Join a team that’s advancing clinical research.

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

Qualifications

• Passionate and driven
• Ability to manage multiple priorities in a fast-paced environment

Skills

• Excellent communication skills
• Strong problem-solving abilities
• Organizational skills

Benefits

• 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

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

Field-based