Remote Clinical Research Associate – Trials Monitor (Phase I–IV)

Remote Clinical Research Associate – Trials Monitor (Phase I–IV)

Full-Time 37900 - 45000 £ / year (est.) Home office (partial)
Novartis Farmacéutica

At a Glance

  • Tasks: Drive trial delivery and ensure data integrity across Phase I–IV clinical trials.
  • Company: Join Novartis Pharmaceuticals, a leader in innovative healthcare solutions.
  • Benefits: Enjoy competitive salary, flexible remote work, and opportunities for professional growth.
  • Other info: Dynamic role with opportunities to work with cross-functional teams.
  • Why this job: Make a real impact in healthcare by ensuring high-quality clinical trials.
  • Qualifications: Experience in clinical research and strong collaboration skills required.

The predicted salary is between 37900 - 45000 £ per year.

Novartis Pharmaceuticals UK Ltd. in London is seeking a Clinical Research Associate to drive trial delivery across Phase I–IV, building site partnerships and ensuring data integrity.

This field-facing role manages monitoring activities, site trainings, and risk mitigation, delivering high-quality trials with integrity and impact.

You will monitor sites on-site and remotely, promote compliance with GCP and ICH guidelines, and collaborate with cross-functional teams.

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Remote Clinical Research Associate – Trials Monitor (Phase I–IV) employer: Novartis Farmacéutica

At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the healthcare sector. Our commitment to employee growth is evident through continuous training and development opportunities, ensuring that our team members can thrive while making a meaningful impact on patient access to life-changing medicines in Southwest England and South London.

Novartis Farmacéutica

Contact Details:

Novartis Farmacéutica Recruitment Team

We think you need these skills to ace Remote Clinical Research Associate – Trials Monitor (Phase I–IV)

Clinical Research
Trial Monitoring
Data Integrity
Site Partnerships
GCP Compliance
ICH Guidelines
Risk Mitigation