CRA 2/Senior CRA 1

IQVIA; Carlsbad (CA); On-site; USD 90,200 - 175,100; Full time

Benefits offered by this job

Opportunities for growth and career development

Collaborative teams

Dynamic, fast-paced environment

Job summary

IQVIA is looking for a Clinical Research Associate (CRA) in Carlsbad, California, to lead various clinical trials and ensure high-quality study execution. The successful candidate will monitor sites, manage study progress, and will have a significant impact on improving patient outcomes.

Candidates should possess a relevant bachelor's degree and at least 1.5 years of on-site monitoring experience. Strong communication, problem-solving, and organizational skills are essential.

Join IQVIA to work collaboratively with experienced teams in a dynamic environment that offers growth and career development opportunities.

Qualifications

• 1.5+ years of on-site monitoring experience.
• Solid understanding of GCP, ICH, and regulatory requirements.

Responsibilities

• Lead and execute site monitoring visits in accordance with GCP/ICH guidelines.
• Build strong relationships with investigative sites to drive performance.
• Track and manage study progress, including regulatory approvals.

Skills

Communication skills

Problem-solving skills

Organizational skills

Ability to manage multiple priorities

Education

Bachelor’s degree in life sciences, healthcare, or related field

Job description

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 elevate 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 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. https://jobs.iqvia.com/eoe

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.

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.