Snabbfakta
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- Manchester
Ansök senast: 2024-11-18
Clinical Research Associate - North UK
Are you passionate about clinical research and ensuring the highest quality standards? Do you have experience in managing clinical trial sites and maintaining compliance with regulations? If so, we have an exciting opportunity for you to join our team as a Clinical Research Associate for the Northern UK.
Apply today for a life-changing career.
For over 100 years we have been driving change to defeat diabetes, but we know that what got us here today is not necessarily what will make us successful in the future. We are now transforming our business and taking our expertise into new territories including obesity and rare blood and endocrine diseases.
Our story is one of incredible growth and success, which has culminated in receiving many prestigious awards, such as Best Places to Work and Vitality – Britain’s Healthiest Workplace.
The position
As a Clinical Research Associate you will manage clinical trial sites to a high quality in accordance with the Company’s policies and procedures, relevant legislation and ICH GCP requirements whilst maintaining the standards of the Novo Nordisk Way. You will act as the main line of communication between the site and the sponsor.
In this role, you will report to Regional Clinical Research Manager- North team.
Your key accountabilities will include:
Complete clinical trial site monitoring visits, reports, and follow-up activities
Provide support and act as a local expert for systems or knowledge areas, sharing best practices for the team's benefit
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
Qualifications
To be successful in this role, you should have the following qualifications:
Degree level qualification in life science or nursing (or equivalent, desirable)
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
About the department
Our Clinical Development Cantres (CDCs), part of the Clinical, Medical and Regulatory Departments, are the backbone in clinical trials and have the benefits of strengthened partnerships and launches. We conduct clinical trials in more than 50 countries around the world, in close collaboration with our affiliates, regions and global teams.
You will be a part of our large, resourceful development team that plays a crucial role in the ambitious drug development programs at Novo Nordisk. The entire Centre consists of around 100 individuals, overseeing 30% of all clinical trial patients in North West Europe.
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