At a Glance
- Tasks: Conduct site monitoring visits and manage study progress for Oncology studies across the UK.
- Company: IQVIA is a leading global provider of clinical research services in the life sciences sector.
- Benefits: Flexibility to travel to sites as required, enhancing work-life balance.
- Other info: Independent on-site monitoring experience for unblinded studies is essential.
- Why this job: Join a mission-driven team focused on creating a healthier world through innovative medical treatments.
- Qualifications: Requires a life science degree or equivalent industry experience in Oncology therapeutic area.
The predicted salary is between 35000 - 45000 £ per year.
IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK.
- 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.
- 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.
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. 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.
Clinical Research Associate (Cra) - Oncology in Suffolk employer: IQVIA
IQVIA, located in the UK, offers a dynamic environment for clinical research professionals. The company focuses on improving patient outcomes and population health worldwide, providing opportunities for impactful work in the life sciences industry. Employees benefit from a commitment to integrity and a zero tolerance policy for candidate fraud.
