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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 Manchester employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CRA 2 - Single Sponsor Dedicated 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 CRA roles. 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 brushing up on your knowledge of GCP and ICH guidelines. Be ready to discuss how you've applied these in your previous roles. We want to see that you can not only talk the talk but also walk the walk!
✨Tip Number 3
Showcase your organisational skills! During interviews, share examples of how you've managed multiple studies or projects simultaneously. Highlighting your time management abilities will make you stand out as a candidate who can handle the demands of a CRA role.
✨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 genuinely interested in joining our mission to drive healthcare forward.
We think you need these skills to ace CRA 2 - Single Sponsor Dedicated in Manchester
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, be ready to discuss how you've established effective lines of communication in past roles. Highlight any strategies you've used to manage expectations and resolve issues promptly.
✨Be Organised and Detail-Oriented
Bring along a well-organised portfolio of your previous work, including visit reports and action plans. This not only shows your attention to detail but also gives you concrete examples to refer to during the interview, making your responses more impactful.
