Clinical Monitor

Clinical Monitor

Full-Time 33000 - 45500 $ / year (est.) Hybrid
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At a Glance

  • Tasks: Conduct site visits, verify trial data, and ensure patient safety in clinical research.
  • Company: Established healthcare organisation in the heart of Cambridge's clinical research hub.
  • Benefits: Competitive salary, hybrid working, private medical insurance, and performance bonuses.
  • Other info: Great career growth opportunities in a thriving research environment.
  • Why this job: Join a dynamic field where your work directly impacts patient care and treatment development.
  • Qualifications: Experience in clinical research and a degree in life sciences or nursing.

The predicted salary is between 33000 - 45500 $ per year.

Perfect role for a mid professional looking to grow their Healthcare career in Cambridge. Cambridge has become one of the UK's genuine centres for clinical research, with a dense cluster of pharmaceutical and biotech organisations running trials that shape how new treatments reach patients. This Clinical Monitor role sits inside that world, with an established healthcare organisation that has the scale, structure and track record to back serious career development. It's a role for someone who wants clear responsibilities and proper frameworks to work within, not a job where you're figuring everything out from scratch.

Here's what you'll be doing:

  • Conducting site visits to verify trial data accuracy, protocol compliance and patient safety standards
  • Reviewing case report forms and source documents against regulatory requirements
  • Building relationships with investigators and site staff to keep studies on track
  • Flagging and escalating protocol deviations before they become bigger problems
  • Preparing monitoring visit reports and maintaining trial master files
  • Supporting site initiation, ongoing monitoring and close-out activities across your assigned portfolio

Here are the skills you'll need:

  • Experience in clinical research, ideally as a Clinical Research Associate or in a similar monitoring capacity
  • Solid understanding of Good Clinical Practice (GCP) and ICH guidelines
  • Sharp attention to detail. Missing a data discrepancy here has real consequences
  • Confident communicator who can hold their own with investigators and site coordinators
  • Comfortable managing multiple sites and competing deadlines at once
  • A degree in life sciences, nursing or a related field

Key perks and benefits:

  • Β£33,000 to Β£45,500, depending on experience
  • Hybrid working, so you're not tied to an office five days a week
  • Private medical and dental insurance
  • Enhanced pension scheme and performance-based bonuses
  • A comprehensive benefits package built for the long term, not just year one

Why pursue a career in Healthcare? Healthcare rewards precision and persistence, and clinical trials are where that shows up most clearly. Cambridge gives you access to a concentration of research activity that few other UK cities can match, which means the Clinical Monitor career path here tends to open doors rather than close them. Get good at this and the next step, whether that's senior monitoring or a move into trial management, is usually within reach.

Clinical Monitor employer: The Opportunity Hub UK Ltd

Join a leading healthcare organisation in Cambridge, a hub for clinical research, where your career as a Clinical Monitor can truly flourish. With a strong focus on employee development, hybrid working options, and a comprehensive benefits package, you'll find a supportive environment that values precision and persistence. This role offers clear responsibilities and the opportunity to build meaningful relationships within the industry, paving the way for future career advancements.

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Contact Details:

The Opportunity Hub UK Ltd Recruitment Team

We think you need these skills to ace Clinical Monitor

Clinical Research Experience
Good Clinical Practice (GCP)
ICH Guidelines Knowledge
Attention to Detail
Communication Skills
Site Management
Time Management