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 40000 - 50000 € 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 employer: IQVIA Laboratories
At IQVIA, we are dedicated to fostering a dynamic work environment that prioritises employee growth and development. As a Clinical Research Associate II in Oncology, you will be part of a collaborative team that values innovation and integrity, offering you the chance to make a meaningful impact in the healthcare sector. With a commitment to continuous learning and a supportive culture, IQVIA provides an excellent platform for advancing your career while contributing to vital research initiatives.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II, Oncology
✨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 open doors and give you insider info on the role.
✨Tip Number 2
Prepare for the interview 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 Clinical Research Associate II role.
✨Tip Number 3
Showcase your experience with site monitoring visits. Be ready to share specific examples of how you've managed multiple clinical trial protocols. This will demonstrate your hands-on expertise and make you stand out!
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Clinical Research Associate II, Oncology
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 knowledge of GCP and ICH guidelines. We want to see how your background aligns with our mission!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Share your passion for clinical research and how you can contribute to our team. Be sure to mention any specific experiences that relate to the responsibilities listed in the job description.
Showcase Your Skills:In your application, don’t forget to showcase your skills in managing multiple clinical trial protocols and your ability to adapt to project needs. We love seeing candidates who can demonstrate flexibility and problem-solving abilities!
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and get you on the path to joining our team at IQVIA!
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
Since the role involves adapting and driving subject recruitment plans, be ready to discuss strategies you've used in the past to enhance recruitment predictability. Share any innovative approaches you’ve taken to engage sites and improve participant enrolment.
✨Communicate Effectively
Effective communication is key in this role. Think about how you’ve established lines of communication with study sites in previous positions. Be prepared to discuss how you manage ongoing project expectations and resolve issues, as this will highlight your collaborative skills.
