Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Manage and monitor clinical sites, ensuring smooth operations and recruitment.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Enjoy a diverse team, advanced tech, and opportunities for growth.
- Why this job: Make a real impact on global health while continuously learning.
- Qualifications: Must have 6 months of independent monitoring experience and a life science degree.
- Other info: This role does not offer UK visa sponsorship.
The predicted salary is between 36000 - 60000 £ per year.
IQVIA Clinical FSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK to join us on our mission to help create a healthier world. By joining our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward. Responsibilities Site management and monitoring (site selection, site initiation, routine monitoring and close-out visits) in partnership with a single-sponsor. Working with sites to adapt, drive and track subject recruitment plan. Providing protocol and study training to assigned sites. Creating and maintain monitoring visit reports and action plans. If appropriate, co-monitoring, training and mentoring junior members of the team. Requirements Experience of independent on-site monitoring in the UK (6 months minimum). 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 as required. Apply today and forge a career with greater purpose, make an impact, and never stop learning! #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 https://jobs.iqvia.com
Senior CRA II employer: Pharmiweb
Contact Detail:
Pharmiweb Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior CRA II
✨Tip Number 1
Make sure to highlight your experience with independent on-site monitoring in the UK. This is a key requirement for the Senior CRA II position, so be prepared to discuss specific examples of your site management and monitoring experiences during the interview.
✨Tip Number 2
Familiarize yourself with the latest Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Being well-versed in these regulations will not only help you in the role but also demonstrate your commitment to maintaining high standards in clinical research.
✨Tip Number 3
Showcase your ability to work collaboratively with sites to adapt and drive subject recruitment plans. Prepare to discuss any successful strategies you've implemented in the past that led to improved recruitment outcomes.
✨Tip Number 4
If you have experience mentoring or training junior team members, be sure to mention it. This role may involve co-monitoring and providing guidance, so demonstrating your leadership skills can set you apart from other candidates.
We think you need these skills to ace Senior CRA II
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Senior CRA II position. Understand the responsibilities and requirements, especially the emphasis on independent on-site monitoring and knowledge of GCP and ICH guidelines.
Tailor Your CV: Customize your CV to highlight relevant experience in clinical research, particularly any independent monitoring roles you've held. Make sure to emphasize your understanding of GCP and ICH guidelines, as well as any life science education.
Craft a Compelling Cover Letter: Write a cover letter that connects your experience with the specific responsibilities outlined in the job description. Mention your ability to manage sites, adapt recruitment plans, and provide training, showcasing how you can contribute to the team.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is clear and professional. A polished application reflects your attention to detail, which is crucial in clinical research.
How to prepare for a job interview at Pharmiweb
✨Showcase Your Monitoring Experience
Be prepared to discuss your previous experience with independent on-site monitoring in the UK. Highlight specific examples of site management, including site selection and initiation, as well as any challenges you faced and how you overcame them.
✨Demonstrate Knowledge of GCP and ICH Guidelines
Make sure to brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Be ready to explain how you have applied these principles in your past roles and how they influence your approach to clinical research.
✨Emphasize Team Collaboration Skills
Since the role involves working closely with sites and potentially mentoring junior team members, be prepared to discuss your teamwork and leadership experiences. Share examples of how you've successfully collaborated with others to achieve common goals.
✨Prepare Questions About the Role and Company
Show your interest in the position by preparing thoughtful questions about the company's mission, the specific responsibilities of the role, and opportunities for professional development. This demonstrates your enthusiasm and commitment to making a positive impact.
