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Responsibilities:

  • Oversee data management activities for clinical trials, ensuring accuracy, integrity, and consistency of all study-related data.
  • Collaborate closely with clinical project managers to align data management processes with study requirements and timelines.
  • Design, develop, validate, and maintain project-specific clinical databases.

Requirements:

  • Bachelor’s or Master’s degree in a scientific field or equivalent experience in data management.
  • Proven experience in data management, preferably within pharmaceutical, biotech, or clinical research environment.
  • Strong proficiency in SQL and experience working with structured databases.

Benefits:

  • Permanent, full-time position with flexible working arrangements (remote within Europe or hybrid in Antwerp).
  • Competitive salary and comprehensive benefits package.
  • Strong emphasis on training, learning, and professional development across technical and soft skills.

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