Clinical Research Associate Job at IQVIA, UK | Life Sciences Candidates, Apply Online
A rare chance has emerged at IQVIA for a Clinical Research Associate Job based in Nottingham, United Kingdom. This full-time, field-based role focuses on supporting Oncology studies across the UK. Interested candidates are encouraged to apply and contribute to a mission aimed at creating a healthier world.
- Job Position: Clinical Research Associate
- Location: Nottingham, United Kingdom
- 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 accelerating the development and commercialization of innovative medical treatments that enhance patient outcomes and improve population health worldwide. With a commitment to integrity and excellence, IQVIA plays a crucial role in the healthcare landscape.
Clinical Research Associate Job Description
The Clinical Research Associate Job will be responsible for performing site monitoring visits, including selection, initiation, monitoring, and close-out visits, in accordance with the contracted scope of work and Good Clinical Practice. The role requires collaboration with sites to adapt and track subject recruitment plans, ensuring effective communication and management of ongoing project expectations.
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 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.
Eligibility Criteria Required For Clinical Research Associate Job
- 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.
Please note – this role is not eligible for visa sponsorship
The opportunity to join IQVIA as a Clinical Research Associate Job offers a chance to make a significant impact in the field of clinical research. Qualified candidates are encouraged to apply before the deadline to embark on a fulfilling career that contributes to global health initiatives.
