At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical trial protocols.
- Company: Join IQVIA, a leader in clinical research and healthcare innovation.
- Benefits: Flexible working, career development, and comprehensive well-being support.
- Other info: Dynamic team environment with opportunities for growth and learning.
- Why this job: Make a real impact on health innovation while advancing your career.
- 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 West 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 at least 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 Bristol employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
