At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with study 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: 12 months of independent 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 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 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.
Research Associate (Immediate Start) in Shrewsbury employer: IQVIA
At IQVIA, we are dedicated to fostering a dynamic work environment that prioritises employee well-being and professional growth. Our South West England team offers flexible working arrangements, comprehensive well-being support, and AI-powered career advancement opportunities, making it an ideal place for passionate individuals to thrive in the clinical research field.
