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 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.
Responsibilities include:
- 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 Calcot employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South East England location provides flexible working arrangements to support a healthy work-life balance, alongside robust career development opportunities through our AI-powered internal talent marketplace. Join us to be part of a mission-driven team dedicated to advancing healthcare while enjoying comprehensive well-being support and the chance to grow your career in a leading global clinical research environment.
