At a Glance
- Tasks: Perform site monitoring visits and manage study progress in accordance with regulatory requirements.
- Company: IQVIA is a leading global provider of clinical research services and healthcare intelligence.
- Benefits: Flexible working options and well-being support for physical, mental, and financial health.
- Other info: Position based in Reading, UK, with opportunities for career advancement through AI-powered tools.
- Why this job: Join a growing team in South East England focused on accelerating innovation in healthcare.
- Qualifications: Requires at least 12 months of independent on-site monitoring experience and a degree in a scientific discipline.
The predicted salary is between 30000 - 40000 £ per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England.
- Career development opportunities to grow as we grow.
- AI-powered career advancement through our internal talent marketplace, Career Connections.
- Flexible working to assist work–life balance and professional success.
- Well-being support covering your physical, mental, and financial health.
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., 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.
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.
Requires at least 12 months independent on-site monitoring experience of interventional studies.
Digital literacy, including confidence using AI tools in a professional setting.
Degree in scientific discipline / health care or equivalent industry experience.
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
Research Associate - Oncology (Reading) in Suffolk employer: IQVIA
IQVIA, located in Reading, UK, offers a mission-driven environment focused on improving patient outcomes. Employees benefit from flexible working arrangements and comprehensive well-being support. The team is dedicated to integrity and innovation in clinical research.
