CRA Oncology Job at IQVIA Biotech | Apply Now
A rare chance for Clinical Research Associates to join IQVIA Biotech in New York, USA. This CRA 2 Oncology Job is a full-time, field-based position seeking professionals with oncology solid tumor monitoring experience. Interested candidates should apply before the deadline.
- Position: CRA 2, Oncology, IQVIA Biotech
- Location: New York, United States of America
- Job Reference: R1567556
About IQVIA Biotech
IQVIA Biotech is a full-service Contract Research Organization (CRO) purpose-built to serve biotech sponsors. With over 25 years of experience, it offers agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. The organization is committed to integrity and excellence in clinical research.
CRA Oncology Job Description
IQVIA Biotech is expanding its Clinical Monitoring team and is seeking CRA 2 professionals with a minimum of 1 year of on-site monitoring experience and oncology solid tumor monitoring experience. The selected candidate will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. This CRA 2 Oncology Job directly contributes to the integrity and quality of clinical research data.
Key Responsibilities
- 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.
Eligibility Criteria for CRA Oncology Job
- Bachelor’s degree in life sciences or related field (or equivalent experience).
- Requires at least 1 year of on-site monitoring experience.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Ability to travel as required by the project.
Salary: The potential base pay range for this role, when annualized, is $74,500.00 – $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).
Qualified candidates are encouraged to apply before the deadline to seize this CRA 2 Oncology Job opportunity at IQVIA Biotech. This role is pivotal in advancing clinical research and contributing to the success of innovative medical treatments.
