Clinical Research Jobs at IQVIA UK
Are you searching for a rewarding clinical research job in oncology within a global CRO? This exciting clinical research associate position in Manchester offers a field-based job in UK with strong career progression through IQVIA Careers. If you are looking for a meaningful job opportunity for life science graduates, this full-time role provides hands-on monitoring experience, exposure to multi-sponsor oncology trials, and the chance to make a real impact on patient outcomes.
About IQVIA
IQVIA is a global provider of clinical research services, healthcare intelligence, and commercial insights to the life sciences and healthcare industries. The organization supports the development and commercialization of innovative medical treatments aimed at improving patient outcomes and population health worldwide.
Job Details:
- Job Title: Clinical Research Associate
- Company: IQVIA
- Location: Manchester, United Kingdom (Field-Based, UK site coverage)
- Employment Type: Full-Time
- Job Reference: R1514135
Clinical Research Job Overview
IQVIA’s Site Management (multi-sponsor) team is seeking a Clinical Research Associate (CRA) to support Oncology studies across the United Kingdom. This field-based role is responsible for ensuring the effective monitoring and execution of clinical trials in compliance with regulatory standards and Good Clinical Practice (GCP).
The Clinical Research Associate will play a critical role in maintaining study integrity, supporting recruitment efforts, and ensuring adherence to protocols and regulatory requirements.
Key Responsibilities
- Conduct site monitoring visits, including selection, initiation, routine monitoring, and close-out visits, in accordance with contracted scope of work and GCP
- Collaborate with study sites to adapt, drive, and track subject recruitment plans in alignment with project timelines
- Deliver protocol and study-related training to assigned sites and maintain consistent communication to manage expectations and address issues
- Evaluate the quality and integrity of site practices related to protocol compliance and regulatory adherence; escalate quality concerns as necessary
- Track study progress, including regulatory submissions and approvals, subject recruitment and enrollment, CRF completion and submission, and data query resolution
- Support study start-up activities as required
- Ensure required documents are filed in the Trial Master File (TMF) and verify that the Investigator Site File (ISF) is maintained in accordance with GCP and local regulations
- Maintain comprehensive documentation of monitoring activities, including visit reports, follow-up letters, and action plans
- Collaborate with study team members to support effective project execution
Requirements for Clinical Research Job
- Experience independently conducting on-site monitoring in the Oncology therapeutic area, including unblinded studies
- In-depth knowledge of Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines
- Degree in Life Sciences or equivalent industry experience
- Flexibility and willingness to travel to study sites as required
- Please note: This role is not eligible for visa sponsorship.
