At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research protocols.
- Company: Join IQVIA, a top-rated global leader in clinical research services.
- Benefits: Competitive salary, career growth, and a supportive learning environment.
- Other info: Flexible travel opportunities and a commitment to continuous learning.
- Why this job: Make a real impact on patient outcomes while working with innovative teams.
- Qualifications: Experience in clinical monitoring and knowledge of GCP and ICH guidelines.
The predicted salary is between 35000 - 45000 £ per year.
Locations: Bath, United Kingdom; Reading, Berkshire, United Kingdom
Time type: Full time
Posted on: Posted Today
Job requisition id: R1540017
Join IQVIA on our mission to accelerate innovation for a healthier world!
IQVIA are seeking experienced Clinical Research Associates in South West England to strengthen our cFSP sponsor-dedicated team.
- We share a passion for the work we do, and the impact it has on customers and patients.
- We are innovative, curious, and feel empowered to explore new ideas and ways of working.
- We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise.
- We are committed to growth, always learning, and making the most of agile career opportunities.
Awards
- IQVIA is a 2026 "Glassdoor Best Place to Work in the UK".
- IQVIA is recognised as #1 in its category on the 2026 Fortune(R) World’s Most Admired Companies(TM) list (for the FIFTH consecutive year!).
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.
- 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.
Please note - this role is not eligible for UK visa sponsorship.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Experienced Clinical Research Associate in Manchester employer: IQVIA LLC
At IQVIA, we pride ourselves on being a leading employer in the clinical research field, offering a dynamic work culture that fosters innovation and collaboration. Our commitment to employee growth is evident through continuous learning opportunities and a supportive environment that encourages exploration of new ideas. Located in the picturesque South West England, our team enjoys a fulfilling career while making a meaningful impact on patient outcomes and healthcare advancements.
StudySmarter Expert Advice🤫
We think this is how you could land Experienced Clinical Research Associate in Manchester
✨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 refer you to someone at IQVIA.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. Make sure you can discuss how your experience aligns with the responsibilities listed in the job description. Confidence is key, so practice makes perfect!
✨Tip Number 3
Show your passion for clinical research during interviews. Share specific examples of how you've contributed to projects in the past and how you can bring that same energy to IQVIA's mission of improving patient outcomes.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're serious about joining our team and making an impact.
We think you need these skills to ace Experienced Clinical Research Associate in Manchester
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight relevant experience, especially in site monitoring and GCP guidelines, so we can see how you fit into our team.
Craft a Compelling Cover Letter:Your cover letter should reflect your passion for clinical research and your understanding of the role. Share specific examples of your past work that align with our mission at IQVIA.
Be Honest and Clear:When filling out your application, honesty is key! We appreciate transparency, so make sure all your information is accurate and complete to avoid any hiccups down the line.
Apply Through Our Website:For the best chance of success, apply directly through our website. This way, we can easily track your application and ensure it reaches the right people in our team!
How to prepare for a job interview at IQVIA LLC
✨Know Your GCP and ICH Guidelines
As an Experienced Clinical Research Associate, it's crucial to have a solid grasp of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Brush up on these regulations before your interview, as you may be asked to discuss how you've applied them in past roles.
✨Showcase Your Monitoring Experience
Be prepared to share specific examples of your independent on-site monitoring experiences. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and adaptability in the field.
✨Emphasise Collaboration Skills
IQVIA values collaboration, so be ready to discuss how you've worked with study teams and sites in the past. Share instances where your communication skills helped manage project expectations or resolve issues, showcasing your ability to work well with others.
✨Prepare Questions About the Role
At the end of the interview, you'll likely have the chance to ask questions. Prepare thoughtful queries about the team dynamics, project expectations, or growth opportunities within IQVIA. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
