CRA 2, Oncology, IQVIA

IQVIA Argentina; Carlsbad (CA); On-site; USD 90,000 - 150,000; Full time

Job summary

IQVIA is seeking a CRA 2 with at least 1.5 years of on-site oncology monitoring experience to perform site visits and ensure adherence to GCP and ICH guidelines. The role involves coordinating subject recruitment plans, training sites, and maintaining documentation across TMF/ISF, with collaboration across the study team.

The ideal candidate has a Bachelor’s degree in a scientific or health-care field and 1.5–2 years of CRA experience, preferably in oncology trials, and is prepared to work

Qualifications

• Bachelor’s Degree in scientific discipline or health care preferred.
• 1.5–2 years of CRA experience including on-site monitoring.
• Experience in oncology trials preferred.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, close-out) per scope and GCP/ICH guidelines.
• Collaborate with sites to adapt and track subject recruitment plans.
• Administer protocol training and maintain regular communication with sites.
• Evaluate site practices for adherence to protocol and regulations; escalate quality issues.
• Track regulatory submissions, recruitment, CRF completion, data queries; may support start-up.
• Maintain TMF/ISF documents; ensure proper filing and regulatory compliance.
• Generate visit reports, follow-up letters, and other study documentation.
• Collaborate with study team for project execution and recruitment planning as needed.

Skills

On-site monitoring

GCP

ICH guidelines

Study coordination

Education

Bachelor’s Degree

Job description

IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience:

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.

Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.

Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Collaborate and liaise with study team members for project execution support as appropriate.

If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.

If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Education: Bachelor’s Degree (Degree in scientific discipline or health care preferred)

Experience: 1.5 to 2 years of relevant CRA experience including on-site monitoring.

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 - $150,400.00. 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.