Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead clinical trial operations and enhance delivery through innovative strategies.
- Company: Join Regeneron, a leader in advancing medical research and innovation.
- Benefits: Comprehensive health benefits, wellness programs, and generous paid time off.
- Why this job: Make a real impact in clinical trials while collaborating with diverse teams.
- Qualifications: 8+ years in clinical trial operations and strong stakeholder relationship skills.
- Other info: Inclusive culture with opportunities for professional growth and travel.
The predicted salary is between 36000 - 60000 £ per year.
At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. We’re looking for a Senior Manager, Global Site Management and monitoring, to join our team and play a pivotal role in coordinating and improving the delivery of clinical trial operations. In this role, you’ll contribute to the planning, execution, and oversight of our clinical trial portfolio, ensuring collaboration among internal teams, external vendors, and investigator sites. With opportunities to drive innovation and process improvement, this position offers meaningful impact in advancing clinical trial strategies and methodologies.
A Typical Day:
- Develop and be responsible for study-specific risk-based monitoring strategies to ensure compliance and efficiency, while managing vendor relationships, including onboarding, performance evaluations and resource alignment.
- Collaborate with Clinical Trial Management teams to design monitoring strategies aligned with RBQM methodologies, including budget planning and approval.
- Provide input to monitoring plans, ensuring alignment with critical data specifications and SDR/SDV approaches.
- Oversee and evaluate performance metrics and risk indicators, providing intervention as needed.
- Act as an SME for monitoring/site management topics, offering guidance to internal and external stakeholders.
- Support inspection readiness activities and participate in regulatory GCP inspections and audits.
This Role May Be For You If:
- You have extensive experience with risk-based quality operating models and clinical trial operations.
- You excel in collaborative environments while maintaining the ability to work independently.
- You are skilled in establishing relationships with stakeholders and translating strategies into actionable frameworks.
- You are familiar with medical terminology and industry regulations, including ICH/GCP standards.
To Be Considered:
- Applicants must have a Bachelor’s Degree and at least 8 years of proven experience in clinical trial operations, monitoring, and site management.
- A proven understanding of ICH/GCP standards and familiarity with medical terminology are crucial.
- Preferred qualifications include experience in risk-based monitoring methodologies and expertise in collaborating with CROs and FSPs.
- This position involves travelling up to 25% of the time to support site management activities.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location.
Senior Manager Global Site Management and Monitoring in Uxbridge employer: Regeneron Pharmaceuticals, Inc.
Contact Detail:
Regeneron Pharmaceuticals, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager Global Site Management and Monitoring in Uxbridge
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to clinical trials. You never know who might have a lead on your dream job at Regeneron!
✨Show Off Your Expertise
When you get the chance to chat with potential employers, don’t hold back! Share your knowledge about risk-based monitoring and clinical trial operations. This will show them you’re not just another candidate, but someone who can truly contribute to their team.
✨Prepare for the Interview
Do your homework on Regeneron and its clinical trial strategies. Be ready to discuss how your experience aligns with their goals. Practising common interview questions can also help you feel more confident when it’s time to shine!
✨Apply Through Our Website
Don’t forget to apply directly 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 being part of the Regeneron team.
We think you need these skills to ace Senior Manager Global Site Management and Monitoring in Uxbridge
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Manager role. Highlight your experience in clinical trial operations and risk-based monitoring methodologies. We want to see how your skills align with 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 this role and how your background makes you a perfect fit. Don’t forget to mention your collaborative spirit and ability to work independently.
Showcase Relevant Experience: When detailing your experience, focus on specific projects or roles where you’ve successfully managed vendor relationships or developed monitoring strategies. We love seeing concrete examples of your impact in previous positions!
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, you’ll find all the info you need about the role and our company culture there!
How to prepare for a job interview at Regeneron Pharmaceuticals, Inc.
✨Know Your Stuff
Make sure you brush up on your knowledge of risk-based quality operating models and clinical trial operations. Familiarise yourself with ICH/GCP standards and medical terminology, as these will likely come up during the interview.
✨Showcase Your Collaboration Skills
Since this role involves working closely with various teams and stakeholders, be prepared to discuss examples of how you've successfully collaborated in the past. Highlight any experiences where you’ve translated strategies into actionable frameworks.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific situations related to monitoring strategies or vendor management. Think about your past experiences and be ready to share how you’ve tackled challenges in clinical trial operations.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the role and the company. Inquire about their current clinical trial portfolio or how they approach innovation and process improvement in site management.
