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: Competitive salary, flexible working hours, and opportunities for professional growth.
- Other info: Field-based role with a focus on collaboration and impactful work.
- Why this job: Make a real difference in cancer research while developing your career in a dynamic field.
- Qualifications: 1+ year of clinical 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 Leeds 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 Leeds, our field-based team provides unique opportunities to engage with cutting-edge oncology research 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 Leeds
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work in oncology. A friendly chat can 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 the right fit for the role.
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications through our website. A quick email or call can keep you on their radar and show your enthusiasm for the position.
✨Tip Number 4
Showcase your monitoring experience! Be ready to share specific examples of how you've handled site visits and resolved issues in past roles. This will help you stand out as a candidate who can hit the ground running.
We think you need these skills to ace Clinical Research Associate II, Oncology in Leeds
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.
✨Build Rapport with the Interviewers
Establishing a connection with your interviewers can go a long way. Be personable and engage them in conversation about their experiences in clinical research. This not only makes you memorable but also shows your ability to build relationships, which is crucial for a Clinical Research Associate.
✨Prepare Questions About the Role
Have a few thoughtful questions ready about the role and the team dynamics. Asking about the challenges they face or how success is measured in this position demonstrates your genuine interest and helps you assess if the company is the right fit for you.
