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For Companies At a Glance
- Tasks: Conduct monitoring visits and ensure compliance with clinical research protocols.
- Company: Join IQVIA, a leader in healthcare innovation and clinical research.
- Benefits: Gain valuable experience in a dynamic environment with growth opportunities.
- Why this job: Make a real impact on patient outcomes while advancing your career in healthcare.
- Qualifications: Bachelor’s degree preferred; 1 year of monitoring experience required.
- Other info: Collaborative team culture focused on driving healthcare forward.
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.
Responsibilities
- Perform monitoring visits (selection, initiation, monitoring and close-out) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plans 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, CRF completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies of 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 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 with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plans on a per-site basis.
- If applicable, may be accountable for site financial management according to the executed clinical trial agreement and retrieve invoices according to local requirements.
Qualifications
- Bachelor’s Degree in a scientific discipline or health care preferred.
- At least 1 year of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of and skill in applying applicable clinical research regulatory requirements (e.g., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of the English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Please note - this role is not eligible for UK visa sponsorship.
CRA 2 - Single Sponsor Dedicated in Reading employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CRA 2 - Single Sponsor Dedicated in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can help you land that CRA role.
✨Tip Number 2
Prepare for interviews by researching the company and understanding their projects. We recommend practising common interview questions and even role-playing with a friend. The more comfortable you are, the better you’ll perform when it’s time to shine!
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the position. We suggest mentioning something specific from the interview to remind them of your conversation and keep you top of mind.
✨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, we often have exclusive roles listed there that you won’t find anywhere else. So, get clicking!
We think you need these skills to ace CRA 2 - Single Sponsor Dedicated in Reading
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the CRA role. Highlight your monitoring experience and any relevant skills that match the job description. 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 clinical research and how you can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Skills: Don’t forget to mention your computer skills and knowledge of GCP and ICH guidelines. We’re looking for someone who can hit the ground running, so make sure we see those skills front and centre in your application.
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, it shows us you’re serious about joining our team!
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. Being able to discuss these in detail will show that you understand the regulatory landscape and can apply it effectively in your role.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous monitoring visits. Talk about how you handled site selection, initiation, and close-out processes. This will help illustrate your hands-on experience and problem-solving skills in real-world scenarios.
✨Showcase Your Communication Skills
Since this role involves regular communication with sites, practice articulating your thoughts clearly. Be ready to discuss how you've established effective lines of communication in past roles and how you manage ongoing project expectations.
✨Be Organised and Detail-Oriented
Bring along any relevant documentation or reports that showcase your organisational skills. Discuss how you track regulatory submissions and manage study documentation, as this will highlight your attention to detail and ability to keep projects on track.
