CRA 2/Senior CRA

IQVIA; Gilbert (AZ); On-site; USD 90,200 - 175,100; Full time

Benefits offered by this job

Opportunities for growth and career development

Dynamic, fast-paced environment

Job summary

IQVIA is seeking a Clinical Research Associate (CRA) with experience in oncology for an onsite role in Gilbert, Arizona. The successful candidate will monitor clinical trials, ensuring compliance and high-quality execution, while collaborating with investigative sites.

Candidates should have a Bachelor’s degree in life sciences and over a year of relevant monitoring experience. The position offers a dynamic work environment and opportunities for career growth.

The potential base pay range is $90,200.00 - $175,100.00 annually.

Qualifications

• 1+ year of on-site monitoring experience required.
• Solid understanding of GCP, ICH, and regulatory requirements is essential.
• Ability to manage multiple priorities in a fast-paced environment.

Responsibilities

• Lead and execute site monitoring visits in accordance with GCP/ICH guidelines.
• Build relationships with investigative sites to drive performance and engagement.
• Ensure protocol compliance, data integrity, and study execution quality.

Skills

On-site monitoring experience

Strong communication skills

Problem-solving skills

Organizational skills

Education

Bachelor’s degree in life sciences

Job description

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

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 expedite 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+ 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

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

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). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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.