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- Tasks: Join our team to monitor clinical sites and ensure compliance with regulations.
- Company: IQVIA is a global leader in clinical research and healthcare intelligence.
- Benefits: Enjoy supportive leadership, collaborative teams, and tech-enabled resources for efficiency.
- Why this job: Grow your career while making a real impact on patient outcomes.
- Qualifications: 6 months+ monitoring experience and a life sciences degree or equivalent.
- Other info: This role requires travel across Scotland and Northern England.
The predicted salary is between 30000 - 42000 £ per year.
We are seeking Clinical Research Associates (CRA I or CRA II) to join our sponsor-dedicated team and support sites across Scotland and Northern England.
Excellent opportunity for CRAs local to Scotland or Northern England who would value:
- Supportive leadership and collaborative teams
- A variety of career opportunities to allow you to grow as we grow
- Technology-enabled resources that make doing your job 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
Requirements
- 6 months + experience of independent on-site monitoring
- Life science degree educated or equivalent industry experience
- Flexibility to travel to sites across Scotland and Northern England
#LI-ADAMTHOMPSON
*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. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Clinical Research Associate - Scotland employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate - Scotland
✨Tip Number 1
Familiarize yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Understanding these regulations will not only help you in your role but also demonstrate your commitment to quality and compliance during interviews.
✨Tip Number 2
Network with current Clinical Research Associates or professionals in the field. Engaging with them can provide insights into the company culture at StudySmarter and may even lead to referrals, which can significantly boost your chances of landing the job.
✨Tip Number 3
Highlight your experience with site monitoring visits in your conversations. Be prepared to discuss specific examples of how you've managed site relationships and addressed challenges, as this will showcase your hands-on experience and problem-solving skills.
✨Tip Number 4
Stay updated on the latest trends and technologies in clinical research. Being knowledgeable about new tools and methodologies can set you apart from other candidates and show that you're proactive about improving efficiency in your work.
We think you need these skills to ace Clinical Research Associate - Scotland
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Clinical Research Associate position. Understand the responsibilities and requirements, especially the importance of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in independent on-site monitoring and any relevant life science education. Be specific about your previous roles and how they relate to the responsibilities outlined in the job description.
Showcase Your Skills: Demonstrate your flexibility and ability to travel across Scotland and Northern England. Mention any technology-enabled resources you have used in previous roles that made your work more efficient, as this aligns with the company's focus on technology.
Tailor Your Application: Customize your application materials to reflect the supportive leadership and collaborative team environment mentioned in the job description. Use language that shows you value teamwork and communication, which are key aspects of the role.
How to prepare for a job interview at IQVIA
✨Know Your GCP and ICH Guidelines
Make sure you are well-versed in Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Being able to discuss these regulations confidently will show that you understand the critical aspects of clinical research.
✨Demonstrate Your Monitoring Experience
Prepare to share specific examples from your previous monitoring experiences. Highlight how you managed site visits, addressed quality issues, and ensured compliance with protocols. This will help illustrate your hands-on experience and problem-solving skills.
✨Showcase Your Communication Skills
As a CRA, you'll need to establish regular lines of communication with sites. Be ready to discuss how you've effectively communicated with stakeholders in the past, and provide examples of how you managed expectations and resolved issues.
✨Express Your Flexibility and Travel Readiness
Since the role requires travel across Scotland and Northern England, express your willingness and flexibility to travel. Share any relevant experiences where you successfully managed travel logistics while maintaining project timelines.
