Clinical Research Associate Job at IQVIA, UK | Life Science Candidates, Apply Online
This Clinical Research Associate job is a rare opportunity to join IQVIA in Nottingham, United Kingdom. This full-time, field-based position focuses on supporting Oncology studies across the UK, offering an opportunity to make a significant impact in the healthcare sector.
- Job Position: Clinical Research Associate
- Location: Nottingham, United Kingdom
- Job Type: Full time, Field-based
- Reference Number: R1514135
About The Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization is dedicated to creating intelligent connections that accelerate the development and commercialization of innovative medical treatments, ultimately aiming to improve patient outcomes and population health worldwide.
Clinical Research Associate Job Description
The Clinical Research Associate will support Oncology studies and cover sites across the UK. This role involves performing site monitoring visits, adapting recruitment plans, and ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.
Clinical Research Associate Job – Key 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 plans 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) 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.
Eligibility Criteria
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- In-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
IQVIA presents a compelling opportunity for qualified candidates to contribute to vital healthcare research. Interested individuals are encouraged to apply at the earliest for this Clinical Research Associate job to make a difference in the field of clinical research.
