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For Companies At a Glance
- Tasks: Monitor clinical trials and ensure compliance with regulations while collaborating with diverse teams.
- Company: Join IQVIA, a top-rated company in healthcare innovation and research.
- Benefits: World-class training, career development, and the chance to work on cutting-edge medicines.
- Why this job: Make a real impact in healthcare and grow your career with purpose.
- Qualifications: 18 months of monitoring experience and knowledge of GCP and ICH guidelines.
- Other info: Flexible travel opportunities and a dynamic work environment await you.
The predicted salary is between 36000 - 60000 £ per year.
Join Us on Our Mission to Drive Healthcare Forward
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.
Do you want to know more about IQVIA? then see what Forbes said about us!
https://www.forbes.com/sites/vijaygurbaxani/2020/11/29/cios-with-vaccines-on-the-horizon-its-time-to-accelerate/?sh=5ca3b83237a1
Why IQVIA?
- IQVIA is recognized as #1 in its category on the 2025 Fortune® World’s Most Admired Companies™ list for the FOURTH consecutive year!
- We offer genuine career development opportunities for those who want to grow as part of the organization.
- The chance to work on cutting edge medicines at the forefront of new medicines development.
- IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
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
- A minimum of 18 months 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!
*Please note – this role is not eligible for UK visa sponsorship*
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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Senior Clinical Research Associate employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching IQVIA and its projects. Familiarise yourself with their recent achievements and how they align with your career goals. This will show your genuine interest and help you stand out during the interview.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to site monitoring and GCP guidelines. We recommend doing mock interviews with friends or mentors to build your confidence.
✨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 serious about joining the team at IQVIA and making a difference in healthcare.
We think you need these skills to ace Senior Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Clinical Research Associate role. Highlight your relevant experience, especially in site monitoring and managing clinical trial protocols. 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 driving healthcare forward and how your skills can contribute to our team. Keep it engaging and personal – we love to see your personality!
Showcase Your Knowledge of GCP and ICH: Since this role requires in-depth knowledge of Good Clinical Practice and International Conference on Harmonization guidelines, make sure to mention any relevant training or experience. We’re looking for candidates who are well-versed in these areas!
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
✨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 truly 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 and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills, which are crucial for a Senior Clinical Research Associate.
✨Understand the Company’s Mission
Take some time to research IQVIA and its mission to drive healthcare forward. Be ready to discuss how your values align with theirs and how you can contribute to their goals. This shows genuine interest and helps you stand out as a candidate who is not just looking for a job, but a purpose.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about the role, team dynamics, and opportunities for professional development. This not only shows your enthusiasm for the position but also helps you gauge if the company is the right fit for you.
