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CRA , Oncology, Full Service

Job in Houston, Harris County, Texas, 77246, USA
Listing for: IQVIA
Full Time position
Listed on 2026-01-27
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research
Salary/Wage Range or Industry Benchmark: 87200 USD Yearly USD 87200.00 YEAR
Job Description & How to Apply Below
Position: CRA 2, Oncology, Full Service, IQVIA

Join to apply for the CRA 2, Oncology, Full Service, IQVIA role at IQVIA
.

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) 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; elevate 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) of 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.
  • 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, if applicable.
Qualifications
  • Education:

    Bachelor’s Degree in a scientific discipline or health care.
  • Experience:

    1.5 to 2 years of relevant CRA experience, including on‑site monitoring.

Potential base pay range: $87,200.00 – $. Actual base pay offered may vary based on qualifications, location, and schedule.

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

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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