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Clinical Research Associate
2 months 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 ensuring the highest quality standards in clinical trials.
Key Responsibilities:- Manage clinical trial sites to a high quality in accordance with company policies, relevant legislation, and ICH GCP requirements.
- Conduct risk-based quality management of sites in accordance with protocol, monitoring plan, SOPs, relevant legislation, and ICH-GCP guidelines.
- Provide support and act as a local expert for systems or knowledge areas, sharing best practices for the team's benefit.
- 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.
- 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.
- Availability to travel approximately 30% of the time throughout Scotland and Northern England.
Our Clinical Development Centres (CDCs) are the backbone in clinical trials, conducting trials in more than 50 countries around the world. We are a global team working together to drive change and defeat diabetes.
What We Offer:- Bonus scheme for reaching 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 care, support, and respect for our people.
