Clinical Research Associate
1 month ago
We are seeking a highly skilled Clinical Research Associate to join our team at Novo Nordisk. As a Clinical Research Associate, you will play a critical role in managing clinical trial sites to ensure high-quality data collection and compliance with regulatory requirements.
Key Responsibilities- Conduct site monitoring visits, reports, and follow-up activities to ensure compliance with protocol, monitoring plan, SOPs, and ICH-GCP guidelines.
- 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 and provide recommendations for improvement.
- Support the Local Trial Manager as needed and provide line of business support.
- 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.
- Expert user of electronic clinical trial systems.
- Availability to travel approximately 30% of the time throughout Scotland and Northern England.
Our Clinical Development Centres (CDCs) are the backbone of clinical trials at Novo Nordisk. We conduct clinical trials in over 50 countries around the world, in close collaboration with our affiliates, regions, and global teams.
What We Offer- Bonus scheme for achieving goals.
- Field-based workplace.
- 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 a transparent, inclusive culture and leadership.
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