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- Tasks: Monitor clinical sites and ensure adherence to protocols for Oncology studies.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, travel opportunities, and contribute to meaningful health outcomes.
- Why this job: Make a real impact on patient health while advancing your career in a dynamic field.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines required.
- Other info: Flexible travel and excellent growth opportunities in a supportive environment.
The predicted salary is between 36000 - 60000 £ per year.
IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK. Apply today and forge a career with greater purpose, make an impact and never stop learning!
Responsibilities:
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- 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:
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
Please note - this role is not eligible for visa sponsorship.
Clinical Research Associate in Nottingham employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate in Nottingham
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working at IQVIA. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of Good Clinical Practice (GCP) and Oncology studies. We want to see your passion and expertise shine through when discussing your experience!
✨Tip Number 3
Showcase your flexibility and willingness to travel. As a Clinical Research Associate, being adaptable is key. Share examples of how you've successfully managed site visits or adapted to changing project needs.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our mission to create a healthier world.
We think you need these skills to ace Clinical Research Associate in Nottingham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in Oncology studies and any relevant skills that match the job description. We want to see how you can make an impact!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background aligns with our mission at IQVIA. Keep it engaging and personal, so we get to know the real you.
Showcase Your GCP Knowledge: Since Good Clinical Practice is key for this role, make sure to mention your understanding and experience with GCP and ICH guidelines. We’re looking for someone who knows their stuff and can ensure quality in our studies.
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and keep track of all the amazing candidates. Plus, it shows you’re serious about joining our team!
How to prepare for a job interview at IQVIA
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of Oncology studies and the specific protocols involved. Being able to discuss recent advancements or challenges in the field will show that you're not just familiar with the basics, but genuinely interested in the area.
✨Master Good Clinical Practice (GCP)
Since GCP is a key part of the role, ensure you can articulate its principles clearly. Prepare examples from your past experiences where you adhered to these guidelines, as this will demonstrate your commitment to quality and compliance.
✨Showcase Your Monitoring Experience
Be ready to discuss your previous experience with site monitoring visits. Highlight specific instances where you successfully managed site relationships or resolved issues, as this will illustrate your ability to handle the responsibilities of the role effectively.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about their current projects or team dynamics. This not only shows your enthusiasm for the position but also helps you gauge if the company culture aligns with your values.