Clinical Data Operations Specialist

1 week ago


Copenhagen, Copenhagen, Denmark Lundbeck AS, H Full time
Job Description:

The successful candidate will be responsible for overseeing the entire data lifecycle, from eCRF setup to study closure. This includes data validation, integration, and management to ensure seamless data flows across all stages of the clinical trial process.

You will work closely with cross-functional teams, including Research and Development, Medical Affairs, and Biometrics, to deliver high-quality clinical trial data that meets regulatory requirements.

  • Data management: Set up and manage electronic Case Report Forms (eCRFs), conduct data validation, and ensure data integrity.
  • Collaboration: Work closely with internal stakeholders to ensure data accuracy, completeness, and compliance.
  • Problem-solving: Identify and resolve data-related issues promptly and effectively.

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