SrCRA, IQVIA Biotech Argentina

IQVIA; Buenos Aires; On-site; ARS 107,614,000 - 138,361,000; Full time

Job summary

IQVIA Biotech in Argentina is hiring a Senior Clinical Research Associate (Sr. CRA) with oncology experience to monitor trial sites and ensure compliance with protocol, regulations and sponsor requirements.

The role involves site visits, recruitment tracking, training delivery, and collaboration with study teams. A Bachelor’s degree and 3–4 years on-site monitoring experience are required, with strong regulatory/GCP knowledge.

Qualifications

• Bachelor’s Degree in scientific discipline or health care preferred.
• Requires at least 3-4 years of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Drive and track subject recruitment plans to enhance project predictability.
• Administer protocol and related study training to assigned sites and establish regular communication to manage expectations and issues.
• Evaluate quality and integrity of site practices and escalate issues as needed.
• Manage progress of studies by tracking regulatory submissions, recruitment, CRF completion, data query handling, and support start-up phase.

Skills

GCP knowledge

Education

Bachelor’s Degree in scientific discipline or health care

Job description

IQVIA Biotech is now hiring for Sr. CRA in Argentina, oncology preferred.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Profile Summary

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Job Functions, Duties and Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• 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. Responsibilities Essential Functions
• 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.

Qualifications

• Bachelor’s Degree in scientific discipline or health care preferred.
• Requires at least 3-4 years of year of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.

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 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.