Clinical Research Program Manager – Monitoring & QA
Clinical Research Program Manager – Monitoring & QA

Clinical Research Program Manager – Monitoring & QA

Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Oversee compliance and quality assurance for clinical trials, ensuring regulatory standards are met.
  • Company: Leading healthcare organisation dedicated to advancing clinical research.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Make a real difference in patient care through impactful clinical research management.
  • Qualifications: Bachelor's degree and significant experience in clinical research required.
  • Other info: Join a dynamic team with a commitment to excellence in healthcare.

The predicted salary is between 36000 - 60000 £ per year.

A leading healthcare organization seeks a Clinical Research Program Manager to oversee compliance and quality assurance for clinical trials. The role involves conducting detailed patient and pharmacy reviews, ensuring adherence to regulatory standards, and serving as the Administrator for the Data and Safety Monitoring Committee.

Candidates should possess a Bachelor's degree and significant experience in clinical research, coupled with strong analytical and leadership skills.

Clinical Research Program Manager – Monitoring & QA employer: Montefiore Health System

As a leading healthcare organization, we pride ourselves on fostering a collaborative and innovative work culture that prioritises employee growth and development. Our Clinical Research Program Manager role offers the opportunity to make a meaningful impact in clinical trials while benefiting from comprehensive training programmes, competitive compensation, and a supportive environment that values work-life balance.
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Contact Detail:

Montefiore Health System Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Research Program Manager – Monitoring & QA

Tip Number 1

Network like a pro! Reach out to your connections in the healthcare and clinical research fields. Attend industry events or webinars to meet potential employers and get your name out there.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of regulatory standards and quality assurance processes. We recommend practising common interview questions related to clinical trials to showcase your expertise.

Tip Number 3

Showcase your leadership skills! Be ready to discuss examples of how you've led teams or projects in the past. This will help demonstrate your capability to manage clinical research programmes effectively.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace Clinical Research Program Manager – Monitoring & QA

Compliance Management
Quality Assurance
Clinical Trials Oversight
Regulatory Standards Knowledge
Data and Safety Monitoring
Analytical Skills
Leadership Skills
Patient Review
Pharmacy Review
Bachelor's Degree in Relevant Field
Experience in Clinical Research

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in clinical research and quality assurance. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects or achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and how your background makes you the perfect fit for our team. Keep it engaging and personal – we love to see your personality!

Showcase Your Analytical Skills: Since this role involves a lot of compliance and monitoring, make sure to highlight any analytical skills or experiences you have. We’re looking for someone who can dive deep into data and ensure everything meets regulatory standards.

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!

How to prepare for a job interview at Montefiore Health System

Know Your Stuff

Make sure you brush up on the latest regulations and standards in clinical research. Familiarise yourself with compliance protocols and quality assurance processes, as these will likely come up during your interview.

Showcase Your Experience

Prepare specific examples from your past roles that highlight your analytical and leadership skills. Think about times when you successfully managed a clinical trial or improved compliance – these stories will make you stand out.

Understand the Role

Dive deep into the job description and understand what the organisation is looking for. Be ready to discuss how your background aligns with their needs, especially regarding patient and pharmacy reviews.

Ask Insightful Questions

Prepare thoughtful questions about the Data and Safety Monitoring Committee and the organisation's approach to quality assurance. This shows your genuine interest in the role and helps you assess if it's the right fit for you.

Clinical Research Program Manager – Monitoring & QA
Montefiore Health System
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