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Clinical Trial Coordinator

2 months ago

Ballerup, Ballerup Kommune, Denmark Novo Nordisk Full time
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 relevant 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, including updating and uploading information, indexing, and quality control of trial documents in our IT Clinical systems.
  • Assist in outsourcing processes, trial budgets, and updating clinical documents such as protocols and protocol amendments.
  • Support the preparation of monitoring guidelines, laboratory manuals, and enrollment updates in close collaboration with trial managers.
  • Collaborate with internal and external stakeholders worldwide to ensure seamless trial execution.
Requirements
  • Broad administrative experience from supportive roles, preferably within the pharmaceutical industry.
  • Proficiency in using IT systems, including Trial Master File systems, and high skills in MS Office, including Excel and Teams.
  • Strong team player with excellent communication and collaboration skills, able to work independently and manage deadlines.
  • Good understanding of clinical trial processes and procedures.
About Novo Nordisk

We are a dynamic company in an ever-changing industry, driven by a passion for innovation and patient care. We strive for excellence, embracing experimentation and continuous learning. Our team is dedicated to making a meaningful impact on the lives of patients worldwide.