At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Join IQVIA, a leader in clinical research with a focus on innovation.
- Benefits: Gain valuable experience in clinical research and enhance your professional skills.
- Other info: Opportunity to work with a dynamic team and grow your career in clinical research.
- Why this job: Make a difference in healthcare by supporting vital clinical studies.
- Qualifications: 1 year of monitoring experience and knowledge of GCP and ICH guidelines required.
The predicted salary is between 30000 - 40000 £ per year.
IQVIA UK’s Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates.
Essential Functions
- 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.
- 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.
Qualifications
- Requires at least 1 year of independent on-site monitoring experience of interventional studies in the UK.
- Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., GCP and ICH guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Please note - this role is not eligible for UK visa sponsorship.
Clinical Monitoring Associate in Ossett employer: IQVIA
IQVIA UK offers a dynamic and supportive work environment for Clinical Monitoring Associates, where you can thrive in your career while contributing to impactful clinical research. With a strong emphasis on professional development, employees benefit from comprehensive training and opportunities for growth within the multi-sponsor Site Management team. Located in the heart of the UK, our collaborative culture fosters innovation and teamwork, making it an excellent place for those seeking meaningful and rewarding employment in the clinical research field.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Monitoring Associate in Ossett
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at IQVIA or similar companies. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. We all know that knowledge is power, so make sure you can confidently discuss how you've applied these in your previous roles. It’ll show you’re the real deal!
✨Tip Number 3
Don’t just wait for job postings; be proactive! Check our website regularly and apply directly through it. This way, you’ll be one of the first to get noticed when new opportunities pop up.
✨Tip Number 4
Follow up after interviews with a thank-you email. It’s a simple gesture that can set you apart from other candidates. Remind them why you’re the perfect fit for the Clinical Monitoring Associate role!
We think you need these skills to ace Clinical Monitoring Associate in Ossett
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Monitoring Associate role. Highlight your relevant experience in site monitoring and your understanding of GCP and ICH guidelines. We want to see how your skills match what we're looking for!
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 your background makes you a great fit for our team. Keep it concise but engaging – we love a good story!
Showcase Your Communication Skills:Since this role involves liaising with various stakeholders, make sure to highlight your communication skills in your application. Whether it's through examples in your CV or your cover letter, show us how you can effectively manage relationships and expectations.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and submit your materials!
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 before your interview. Being able to discuss these regulations confidently will show that you understand the essential functions of the role and can apply them in practice.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous monitoring visits, highlighting how you handled site selection, initiation, and close-out visits. This will help you illustrate your independent on-site monitoring experience and how it aligns with the job requirements.
✨Showcase Your Communication Skills
Since the role involves establishing regular lines of communication with sites, be ready to discuss how you've effectively managed ongoing project expectations and issues in the past. Think of instances where your communication made a difference in project outcomes.
✨Be Ready to Discuss Problem-Solving
Prepare to talk about how you've evaluated the quality and integrity of study site practices. Have examples ready where you identified quality issues and escalated them appropriately, demonstrating your proactive approach to maintaining high standards in clinical research.
