At a Glance
- Tasks: Monitor clinical trials and ensure compliance with regulations while supporting innovative healthcare solutions.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Flexible working, career development, and well-being support for a balanced lifestyle.
- Other info: Dynamic team environment with opportunities for growth and professional success.
- Why this job: Make a real difference in healthcare by accelerating innovation and improving patient outcomes.
- Qualifications: 2 years of clinical monitoring experience and a degree in a scientific discipline.
The predicted salary is between 35000 - 45000 £ 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:
- 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 2 years 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.
Research Fellow (Clinical Trials) in Westminster employer: IQVIA
At IQVIA, we are dedicated to fostering a dynamic work environment that prioritises employee well-being and professional growth. Our South East England team offers flexible working arrangements, comprehensive support for your physical, mental, and financial health, and AI-driven career advancement opportunities through our internal talent marketplace. Join us in making a meaningful impact on global health while enjoying a collaborative culture that values innovation and integrity.
