Clinical Trial Coordinator
1 week ago
About the Role
We are seeking a highly organized and detail-oriented Clinical Trial Administrator to join our Early Clinical Operations team in a one-year maternity cover. As a key member of our team, you will play a crucial role in supporting the trials in all aspects of study start-up, conduct, documentation, and archiving.
Key Responsibilities
- Establish and maintain Trial Master Files in accordance with standard operational procedures (SOP) on different trials.
- Update and upload information, index, and quality control trial documents in our IT Clinical systems.
- Assist in outsourcing processes, trial budgets, and updating clinical documents such as protocols and protocol amendments.
- Support meeting planning and collaborate with internal and external stakeholders worldwide.
Requirements
- Broad administrative experience from supportive roles, preferably within the pharmaceutical industry.
- Flair for using IT systems and knowledge of Trial Master File systems, as well as high skills in MS Office, including Excel and Teams.
- Strong team player, able to work independently, and well-structured with a sense for detail and a good overview.
- Good collaboration skills and a good sense of humor.
- Proficient in both written and spoken English.
About Novo Nordisk
We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessary what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we're all working to move the needle on patient care.
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