At a Glance
- Tasks: Monitor clinical sites and ensure compliance with regulations while supporting innovative oncology studies.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Competitive salary, professional development, and a chance to make a real impact.
- Other info: Dynamic team environment with opportunities for growth in clinical research.
- Why this job: Be part of a mission to accelerate health innovations and improve patient outcomes.
- Qualifications: 1 year of monitoring experience and knowledge of GCP and ICH guidelines required.
The predicted salary is between 37000 - 45000 € per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! 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 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., GCP and 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 Royal Tunbridge Wells employer: IQVIA Laboratories
At IQVIA, we pride ourselves on fostering a collaborative and innovative work environment that empowers our Clinical Research Associates to thrive. With a strong commitment to employee development, we offer extensive training and growth opportunities, ensuring that our team members are equipped to make a meaningful impact in the field of oncology research. Located in the UK, our Site Management team is dedicated to advancing healthcare solutions while supporting a culture of excellence and integrity.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II, Oncology in Royal Tunbridge Wells
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at IQVIA or similar companies. A friendly chat can sometimes lead to insider info about job openings or even a referral!
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. We all know that knowledge is power, so being able to discuss these topics confidently will show you're serious about the role and ready to hit the ground running.
✨Tip Number 3
Don’t just wait for job alerts! Regularly check our website for new openings and apply directly. The sooner you get your application in, the better your chances of standing out from the crowd.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Plus, it shows your enthusiasm for the position and helps build a positive rapport with the hiring team.
We think you need these skills to ace Clinical Research Associate II, Oncology in Royal Tunbridge Wells
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 and how your previous experiences make you a great fit for our team. Keep it concise but impactful – we love a good story!
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 or 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 you’re keen on joining our mission to accelerate innovation for a healthier world!
How to prepare for a job interview at IQVIA Laboratories
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines before your interview. Being able to discuss these regulations confidently will show that you understand the core of clinical research and can apply them effectively in your role.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous roles where you performed site monitoring visits. Highlight your experience with selection, initiation, monitoring, and close-out visits, as well as how you managed any challenges that arose during these processes.
✨Showcase Your Communication Skills
Since this role involves liaising with various stakeholders, be ready to discuss how you've established effective communication lines in past projects. Share instances where you adapted your communication style to suit different audiences, whether they were site staff or team members.
✨Be Ready to Discuss Recruitment Strategies
IQVIA is looking for someone who can enhance subject recruitment plans. Think about how you've contributed to recruitment efforts in the past and be prepared to share your ideas on how to drive and track recruitment effectively in line with project needs.
