(Senior) Clinical Research Associate, IQVIA

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