CRA , Internal Medicine, Biotech

IQVIA Biotech is seeking CRA 2 candidates with a minimum of 1 year of on-site monitoring experience in internal medicine and/or neurology.

We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.

• Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.

• Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.

• Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.

• Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.

• Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.

• Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.

• Document site management activities, visit outcomes, and follow‑up actions through detailed reports and correspondence.

• Work closely with cross‑functional project teams to support study execution and ensure alignment with project goals.

• Depending on the project, you may also support site‑level recruitment planning and financial management, including invoice collection and budget tracking.

• Bachelor's Degree required. Preferred in scientific discipline or health care. Requires at least 1 year of on-site monitoring experience. Equivalent combination of education, training and experience may be accepted in lieu of degree.

• Strong understanding of GCP, ICH guidelines, and regulatory requirements.

• Ability to travel as required by the project.

The potential base pay range for this role, when annualized, is $87,200.00 - $. 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.

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