Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical protocols.
- Company: Join IQVIA, a top-rated global leader in clinical research services.
- Benefits: Competitive salary, growth opportunities, and a collaborative work environment.
- Why this job: Make a real impact on patient outcomes while advancing your career.
- Qualifications: Experience in clinical monitoring and knowledge of GCP and ICH guidelines.
- Other info: Flexible travel required; not eligible for UK visa sponsorship.
The predicted salary is between 35000 - 45000 £ per year.
We are seeking experienced Clinical Research Associates in Scotland 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.
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 Livingston employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clinical Research Associate in Livingston
✨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 the company and its projects. Show that you’re not just interested in any job, but specifically in how you can contribute to their mission of improving patient outcomes.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to GCP and ICH guidelines. Being able to articulate your knowledge confidently can set you apart from other candidates.
✨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 at IQVIA.
We think you need these skills to ace Experienced Clinical Research Associate in Livingston
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your relevant experience, especially in site monitoring and GCP compliance. We want to see how your skills align with our mission!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Share your passion for clinical research and how you can contribute to our team. Be genuine and let us know why you’re excited about this opportunity at IQVIA.
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you’ve improved processes or outcomes in previous roles. We love to see results-driven candidates!
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 innovative 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
Since the role involves working closely with study teams and site staff, be ready to discuss your collaboration experiences. Share instances where you successfully communicated project expectations or resolved issues, showcasing your ability to work well with diverse teams.
✨Prepare Questions About the Role
Interviews are a two-way street! Prepare thoughtful questions about the company's approach to clinical research and how they support their Clinical Research Associates. This shows your genuine interest in the role and helps you assess if it's the right fit for you.