At a Glance
- Tasks: Monitor clinical sites, ensuring compliance and quality in oncology studies.
- Company: Join a leading global healthcare company dedicated to improving patient outcomes.
- Benefits: Full-time role with competitive salary and opportunities for professional growth.
- Other info: Field-based position with dynamic team collaboration.
- Why this job: Make a real difference in cancer research while developing your career.
- Qualifications: 1 year of monitoring experience and knowledge of GCP and ICH guidelines.
The predicted salary is between 37000 - 45000 £ per year.
IQVIA UK’s Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates.
Essential Functions
- 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 Harmonisation (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.
- 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.
Qualifications
- Requires at least 1 year of independent on‑site monitoring experience of interventional studies in the UK.
- Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Please note - this role is not eligible for UK visa sponsorship.
Clinical Research Associate II, Oncology in Nottingham employer: IQVIA Argentina
IQVIA is an exceptional employer for Clinical Research Associates, offering a dynamic work culture that prioritises collaboration and professional growth. Located in Nottingham, our field-based team provides unique opportunities to engage with cutting-edge oncology studies while benefiting from comprehensive training and support. Employees enjoy a strong emphasis on work-life balance and the chance to make a meaningful impact in the healthcare sector.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II, Oncology in Nottingham
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry events. We all know that sometimes it’s not just what you know, but who you know that can help you land that Clinical Research Associate role.
✨Tip Number 2
Prepare for those interviews by brushing up on your GCP and ICH guidelines knowledge. We recommend doing mock interviews with friends or using online platforms to get comfortable discussing your experience and how it relates to the job.
✨Tip Number 3
Showcase your monitoring experience! When you get the chance to chat with recruiters or during interviews, highlight specific examples of your site monitoring visits and how you’ve tackled challenges in previous roles. We want to see your problem-solving skills in action!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Clinical Research Associate II, Oncology in Nottingham
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate II role. Highlight your relevant experience in site monitoring and your understanding of GCP and ICH guidelines. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about oncology research and how your previous experiences have prepared you for this role. Let us know what excites you about working with our team!
Showcase Your Communication Skills:As a Clinical Research Associate, communication is key. In your application, demonstrate your ability to establish effective working relationships. Share examples of how you've successfully managed project expectations and resolved issues in the past.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at IQVIA Argentina
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines. Being able to discuss these in detail will show that you’re not just familiar with the regulations but can apply them effectively in your role.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your past experience where you successfully performed site monitoring visits. Highlight how you managed recruitment plans or resolved issues, as this will showcase your hands-on expertise and problem-solving skills.
✨Showcase Your Communication Skills
Since this role involves liaising with various stakeholders, be ready to discuss how you establish and maintain effective working relationships. Share instances where your communication made a difference in project outcomes, as this is crucial for success in this position.
✨Be Ready for Scenario Questions
Expect scenario-based questions that test your ability to handle real-life challenges in clinical research. Think about potential quality issues you might encounter and how you would escalate them appropriately, demonstrating your critical thinking and decision-making skills.
