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- Tasks: Monitor clinical trials and ensure compliance with regulations while collaborating with diverse teams.
- Company: Join IQVIA, a top-rated company driving healthcare innovation.
- Benefits: Remote work, career development, and the chance to impact patient outcomes.
- Why this job: Be at the forefront of new medicine development and make a real difference.
- Qualifications: Experience in clinical trial monitoring and knowledge of GCP and ICH guidelines.
- Other info: Flexible travel opportunities and a dynamic work environment.
The predicted salary is between 28800 - 48000 £ per year.
Locations: Reading, Berkshire, United Kingdom
Time type: Full time
Posted on: Posted Today
Job requisition id: R1511546
Join IQVIA on Our Mission to Drive Healthcare Forward! IQVIA's Real World Evidence team are seeking a Clinical Research Associate II. The position is UK based and offers remote working with travel to sites across the UK and Ireland.
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.
- You have 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 science degree educated or equivalent industry experience.
- Flexibility to travel to sites.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Clinical Research Associate, Real World Evidence employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate, Real World Evidence
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Show us you’re genuinely interested in IQVIA’s mission and how you can contribute to driving healthcare forward.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to GCP and ICH guidelines. We want to see that you know your stuff and can handle the responsibilities of a Clinical Research Associate.
✨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 us you’re serious about joining our team.
We think you need these skills to ace Clinical Research Associate, Real World Evidence
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience with GCP and ICH guidelines, as well as any relevant clinical trial management you've done. We want to see how your background fits 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 clinical research and how you can contribute to our Real World Evidence team. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Skills: In your application, don’t forget to showcase your skills in site monitoring and project management. Mention specific examples of how you've successfully managed multiple clinical trial protocols. We’re looking for those standout moments that demonstrate your expertise!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details you need about the role and our company culture there!
How to prepare for a job interview at IQVIA LLC
✨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 of your previous site monitoring experiences. Talk about how you managed multiple clinical trial protocols and the challenges you faced. This will demonstrate your ability to handle the responsibilities of a Clinical Research Associate effectively.
✨Understand the Recruitment Process
Since the role involves enhancing subject recruitment plans, be ready to discuss strategies you've used in the past. Highlight any successful recruitment initiatives you've led or contributed to, as this will show your proactive approach to project needs.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s current projects and future goals. This not only shows your interest in the role but also gives you a chance to assess if the company aligns with your career aspirations. It’s a two-way street!