At a Glance
- Tasks: Monitor clinical trials, ensuring compliance and quality at various sites.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Competitive salary, opportunities for growth, and a chance to make a real impact.
- Other info: Dynamic role with travel opportunities and a focus on continuous learning.
- Why this job: Be part of a mission to accelerate health innovations and improve lives.
- Qualifications: Experience in clinical monitoring 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 team is growing and seeking experienced Clinical Research Associates. 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 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
- Experience of independent on‑site monitoring.
- Successfully managed multiple clinical trial protocols across diverse investigative sites.
- In‑depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life sciences degree educated or equivalent industry experience.
- Flexibility to travel to sites.
Please note - this role is not eligible for UK visa sponsorship.
Clinical Research Associate II, Oncology in Chesterfield employer: IQVIA Laboratories
At IQVIA, we are dedicated to fostering a dynamic work environment that prioritises employee growth and innovation. As a Clinical Research Associate II in Oncology, you will be part of a collaborative team that values your contributions and offers continuous learning opportunities, all while making a meaningful impact on global health. Our UK Site Management team is committed to excellence, ensuring that you have the resources and support needed to thrive in your role.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II, Oncology in Chesterfield
✨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 make sure you can confidently discuss how you've applied these principles in your previous roles.
✨Tip Number 3
Showcase your adaptability! In the fast-paced world of clinical trials, being flexible is key. Share examples of how you've successfully managed multiple protocols or adapted to changing project needs during your interviews.
✨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 genuinely interested in joining our mission to accelerate innovation for a healthier world!
We think you need these skills to ace Clinical Research Associate II, Oncology in Chesterfield
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate II role. Highlight your experience with site monitoring and any relevant clinical trial protocols you've managed. We want to see how your background aligns with our mission!
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 skills can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your GCP Knowledge:Since GCP and ICH guidelines are crucial for this role, make sure to mention your in-depth knowledge of these regulations in your application. We’re looking for candidates who understand the importance of compliance in clinical research.
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 shows you’re serious about joining our mission!
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 Harmonization (ICH) guidelines before your interview. Being able to discuss these in detail will show that you’re not just familiar with them, but that you understand their importance in clinical research.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past roles where you successfully managed multiple clinical trial protocols. Highlight any challenges you faced during site monitoring visits and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills.
✨Understand the Recruitment Process
Familiarise yourself with strategies for enhancing subject recruitment. Be ready to discuss how you’ve adapted or driven recruitment plans in previous roles. This shows that you can think critically about project needs and contribute to the team’s success.
✨Communicate Effectively
Since regular communication with sites is key, practice articulating how you establish and maintain these lines of communication. Think of examples where your communication skills helped resolve issues or improved project expectations. This will highlight your collaborative approach.
