Clinical Data Manager - Home Office

Sep 10, 2022
Oct 10, 2022
Full Time
Clinical Data Manager - Home Office

Remote - Europe

The Emmes Company, LLC ("Emmes") is a global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public health and biopharmaceutical innovation. We believe in the power of truth, so much so that we named our company Emmes, which means truth. Through decades of experience we have learned that collaborative relationships thrive and human health benefits when truth is our compass.

Our "Character Achieves Results" culture is driven by five key values that guide our actions in the way we conduct research and distinguish us as an organization: Integrity, Agility, Passion for Excellence, Collaborative Partnerships and Intellectual Curiosity. We are a trusted partner to clients who share our passion for improving public health in a world of ever-changing scientific research.

If you share our motivations and passion in research, come join us! You will be joining a collaborative culture that empowers every Emmes employee — from entry level through top executive — to contribute to our clients' success by sharing ideas openly and honestly.

Primary Purpose

The Clinical Data Manager is responsible for assisting with data management activities for research studies. You will work as an integral part of a cross-functional team through the lifecycle of the research study from design through final analysis and study closeout. You will be responsible for the completeness and accuracy of the study data in the electronic database and collaborates primarily with internal project teams on all aspects of data collection.

  • Manage all aspects of a global clinical study data management process from start-up to the database lock.
  • Provide support for regulatory submissions.
  • Manage the selection process for a Global Electronic Data Capture (EDC) system for clinical studies.
  • Plan, design, validate, verify and implement database or EDC systems to support clinical studies globally from a data management perspective.
  • Review and contribute to clinical protocols/amendments, clinical study reports, statistical analysis plans, etc.
  • Review and advise on Case Report Forms (CRF) completion guidelines, prepare external data transfer specifications and other study documentation related to data management.

  • Bachelor's or University Degree in health, clinical, biological, chemical or mathematical sciences, or related field.
  • Data Management experience is an advantage.
  • Fluent in English, both written and verbal.

We offer
  • 25 vacation days.
  • Friendly and collaborative working environment.
  • Flexible working hours.
  • Training in Data management.
  • Opportunity to acquire new skills and knowledge.


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