CRA 2/Senior CRA

IQVIA; Carlsbad (CA); On-site; USD 87,200 - 169,300; Full time

Benefits offered by this job

Opportunities for growth and career development

Dynamic, fast-paced environment

Job summary

IQVIA is seeking a passionate Clinical Research Associate (CRA) to ensure high-quality clinical trial execution. This role involves leading site monitoring visits, maintaining compliance with guidelines, and building strong relationships with investigative sites.

Qualified candidates will hold a Bachelor’s in life sciences and have 1+ year of monitoring experience. The position offers a potential salary range of $87,200 to $169,300, along with opportunities for growth and professional development in a dynamic environment.

Qualifications

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

Responsibilities

• Lead and execute site monitoring visits in accordance with GCP guidelines.
• Build strong relationships with investigative sites.
• Ensure protocol compliance and high-quality study execution.
• Identify risks and resolve issues proactively.
• Track study progress and maintain accurate documentation.

Skills

Strong communication skills

Problem-solving skills

Organizational skills

Ability to manage multiple priorities

Solid understanding of GCP and ICH

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 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+ 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

Compensation

The potential base pay range for this role, when annualized, is $87,200.00 - $169,300.00. The actual base pay offered may vary based on 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.

Equal Opportunity Employer

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.

Integrity Statement

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.