Clinical Research Associate Job at IQVIA, UK | Life Science Candidates, Apply Now
A rare chance has emerged for aspiring IQVIA Clinical Research Associate candidates in Reading, United Kingdom. IQVIA is seeking a dedicated professional to support Oncology studies and cover sites across the UK. This full-time, field-based role offers an opportunity to contribute to creating a healthier world.
- Job Position: Clinical Research Associate
- Location: Reading, 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 committed to accelerating the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
IQVIA Clinical Research Associate Job Description
The IQVIA Clinical Research Associate will play a vital role in performing site monitoring visits, managing ongoing project expectations, and ensuring compliance with Good Clinical Practice. This role requires a proactive approach to site management and collaboration with study team members for effective project execution.
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. 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
- 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.
This IQVIA Clinical Research Associate opportunity is designed for motivated individuals eager to make a significant impact in the field of clinical research. Interested candidates are encouraged to apply before the deadline to seize this chance to contribute to vital healthcare advancements.
