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Clinical Research Associate

2 months ago

Manchester, United Kingdom Novo Nordisk Full time
About the Role

We are seeking a highly skilled Clinical Research Associate to join our team at Novo Nordisk. As a key member of our Clinical Development Centre, you will play a crucial role in ensuring the successful execution of clinical trials in accordance with ICH GCP guidelines.

Key Responsibilities
  • Conduct site monitoring visits, reports, and follow-up activities to ensure high-quality data collection and compliance with regulatory requirements.
  • Provide support and act as a local expert for systems or knowledge areas, sharing best practices with the team.
  • Conduct risk-based quality management of sites in accordance with protocol, monitoring plan, SOPs, relevant legislation, and ICH-GCP guidelines.
  • Support the Local Trial Manager as needed and provide line of business support.
Requirements
  • Degree-level qualification in life science or nursing (or equivalent).
  • At least 2 years of experience and success in independently monitoring clinical trials in accordance with ICH GCP methodology.
  • Experience in managing trial management activities for commercial clinical trials and monitoring all phases (1-4) of clinical trials.
  • Expert user of electronic clinical trial systems.
What We Offer
  • Bonus scheme for achieving goals.
  • Market-leading pension scheme with generous employer contributions.
  • Award-winning Wellness programme, including Private Medical Insurance, the Lifeworks App, and wellbeing initiatives.
  • Private medical, life, and disability insurance.
  • Inclusive culture with care, support, and respect for our people.