Clinical Research Associate Job at IQVIA, UK | Life Sciences | Apply Now
Are you an experienced clinical monitor passionate about advancing cancer treatments? Securing this field-based Clinical Research Associate Job at IQVIA is an exceptional opportunity to support critical oncology studies across the United Kingdom. If you are seeking a highly purposeful Life Sciences Job, this role offers the chance to forge a meaningful IQVIA Career while making a direct impact on patient health and predictability in clinical trials.
- Job Position: Clinical Research Associate
- Location: Reading, United Kingdom
- Job ID: R1514135
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. By creating “intelligent connections,” IQVIA accelerates the development and commercialization of innovative medical treatments. Joining the multi-sponsor Site Management team means you will be stepping into an IQVIA Career with a clear mission: to help create a healthier world. You will be supported by a global infrastructure that encourages you to never stop learning, giving you the tools to forge a career with greater purpose and operational impact.
Key Responsibilities
As a Clinical Research Associate supporting vital oncology studies, you will be the primary operational link between the sponsors and the research sites. Your day-to-day duties will require meticulous oversight and strategic relationship-building.
- Lifecycle Monitoring: Perform comprehensive site monitoring visits, including selection, initiation, routine monitoring, and close-out visits, strictly in accordance with contracted scopes of work and Good Clinical Practice (GCP).
- Recruitment & Strategy: Work proactively with sites to adapt, drive, and track subject recruitment plans. Aligning these with project needs is critical to enhancing trial predictability.
- Site Training & Communication: Administer protocol and related study training to assigned sites. You will establish regular lines of communication to manage ongoing project expectations and resolve issues swiftly.
- Quality Assurance: Evaluate the quality and integrity of study site practices. You will ensure proper protocol conduct and escalate quality issues appropriately.
- Operational Tracking: Manage the progress of assigned studies by tracking regulatory submissions, recruitment, enrollment, case report form (CRF) completion, and data query resolution.
- Documentation & Compliance: Verify that the Investigator’s Site File (ISF) is maintained correctly and ensure that all required site documents are filed in the Trial Master File (TMF).
- Reporting: Create and maintain appropriate documentation regarding site management, submitting regular visit reports and generating follow-up letters.
Qualifications & Expertise Required For Clinical Research Associate Job
To succeed in this highly specialized Clinical Research Associate Job, you must bring a strong background in oncology monitoring and clinical compliance.
- Targeted Experience: Proven experience in independent, on-site monitoring within the Oncology therapeutic area specifically for unblinded studies.
- Regulatory Mastery: In-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Educational Foundation: A degree in Life Sciences or equivalent industry experience is required to provide the scientific literacy needed for this Life Sciences Job.
- Mobility: Flexibility to travel frequently to clinical sites across the UK as required by project demands.
- Right to Work: Please note that this role is not eligible for visa sponsorship. Candidates must have the existing right to work in the UK.
In summary, this field-based Clinical Research Associate Job is a definitive career milestone for monitors specializing in oncology. By taking on this Life Sciences Job, you will directly ensure the safety and efficacy of groundbreaking cancer therapies. If you possess the required unblinded oncology experience and the flexibility to travel across the UK, apply today to elevate your IQVIA Career and help bring innovative treatments to patients who need them most.
