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- Tasks: Monitor clinical trials, ensuring compliance and quality at investigative sites.
- Company: Join IQVIA, a top-rated company in healthcare innovation.
- Benefits: World-class training, career development, and the chance to impact healthcare.
- Why this job: Be at the forefront of new medicines and make a real difference.
- Qualifications: 18 months of monitoring experience and a life sciences degree or equivalent.
- Other info: Flexible travel required; no UK visa sponsorship available.
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.
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, driving performance of sites and making the CRA role more efficient.
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.
Senior Clinical Research Associate in Reading employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching IQVIA and understanding their mission. Familiarise yourself with their recent projects and achievements. This will help you tailor your answers and show that you're genuinely interested in being part of their team.
✨Tip Number 3
Practice your interview skills with a friend or mentor. Focus on articulating your experience with GCP and ICH guidelines, as well as your ability to manage multiple clinical trial protocols. Confidence is key, so get comfortable talking about your strengths!
✨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 IQVIA and ready to drive healthcare forward with us.
We think you need these skills to ace Senior Clinical Research Associate in Reading
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 a good story!
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: Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. 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 meaningful career.
✨Prepare Questions for Them
Interviews are a two-way street, so come prepared with thoughtful questions about the role, team dynamics, and company culture. This not only shows your enthusiasm but also helps you gauge if this is the right fit for you. Ask about their approach to site selection and recruitment, as it ties directly into your responsibilities.