At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Join IQVIA, a leader in clinical research and healthcare innovation.
- Benefits: Flexible working, career development, well-being support, and mentorship opportunities.
- Other info: Be part of a team recognised as one of the best places to work!
- Why this job: Make a real impact in healthcare while advancing your career in a supportive environment.
- Qualifications: 2 years of 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's Site Management (full service / multi-sponsor) team is growing and seeking experienced Clinical Research Associates across the UK & Ireland.
Why IQVIA?
- Genuine career development opportunities to grow as we grow
- AI‐powered career advancement through our internal talent marketplace, Career Connections
- Mentorship opportunities across the organisation via Employee Resource Groups
- Flexible working to assist work–life balance and professional success
- Well‐being support covering your physical, mental, and financial health
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- 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. May support start-up phase
- 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
Requirements
- Requires at least 2 years on-site monitoring experience of interventional studies
- Degree in scientific discipline or health care or equivalent industry experience
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Ability to establish and maintain effective working relationships with coworkers and clients
- Full driving license and access to vehicle required for travel to sites
Please note - this position is not eligible for visa sponsorship.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Research Associate – Oncology (Hulme) in Wigan employer: IQVIA
At IQVIA, we are dedicated to fostering a supportive and innovative work environment that prioritises your professional growth and well-being. As a Research Associate in Oncology, you will benefit from flexible working arrangements, comprehensive well-being support, and access to our AI-powered career advancement tools, all while contributing to meaningful projects that enhance patient outcomes. Join us in Hulme and be part of a team recognised as one of the best places to work, where your contributions truly make a difference.
