At a Glance
- Tasks: Monitor clinical sites and ensure compliance with research protocols and regulations.
- 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 and collaboration.
- Why this job: Be part of groundbreaking oncology research that improves patient outcomes.
- Qualifications: 1 year of monitoring experience and knowledge of GCP and ICH guidelines.
The predicted salary is between 35000 - 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 Kent 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 within the dynamic field of oncology research. Located in the UK, our team enjoys a supportive culture that values work-life balance and encourages meaningful contributions to advancing healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II, Oncology in Kent
✨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 with a thank-you email. It’s a simple gesture that shows your appreciation and keeps you fresh in their minds. Plus, it’s a great opportunity to reiterate your enthusiasm for the role!
We think you need these skills to ace Clinical Research Associate II, Oncology in Kent
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 have prepared you for this role. Let us know what excites you about joining IQVIA!
Showcase Your Communication Skills:Since this role involves liaising with various stakeholders, make sure to demonstrate your communication skills in your application. Whether it's through your CV or cover letter, we want to see how you can effectively manage ongoing project expectations.
Apply Through Our Website:Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about our mission and values!
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. Being able to discuss these in detail will show that you’re not just familiar with them, but that you can apply them effectively in your role.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous roles where you successfully conducted site monitoring visits. Highlight your ability to manage the entire process from selection to close-out, as this will resonate well with the interviewers.
✨Showcase Your Communication Skills
Since the role involves liaising with various stakeholders, be ready to discuss how you’ve established effective communication lines in past projects. Share instances where your communication helped resolve issues or improved project outcomes.
✨Be Ready for Scenario Questions
Expect scenario-based questions that test your problem-solving skills. Think of situations where you had to escalate quality issues or adapt recruitment plans, and explain how you handled them. This will demonstrate your critical thinking and adaptability.
