CRA 2/Senior CRA 1
IQVIA
CRA 2/Senior CRA 1
Indianapolis, United States of America | Full time | Field-based | R1547445
Join a team that's advancing clinical research.
We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you'll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.
What you'll do:
- 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
What you bring:
- 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
Why join us:
- 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 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$90.2k - $175.1k
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