Clinical Data Manager

Full Time

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At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world’s most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.

Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we’re working at the pace of change on diagnostic tools that address the world’s biggest health challenges, driven by knowing that behind every test there is a patient waiting.

Learn about the Danaher Business System which makes everything possible.

The Clinical Data Manager, reporting to the Manager or Director of Clinical Data Management, has responsibilities for collaborating with various departments on the design, documentation, testing and implementation of clinical databases to support clinical studies.

This position is part of the Clinical Affairs department and will be located in Solna, Stockholm, Sweden.

In This Role, You Will Have The Opportunity To

 

  • Be responsible for all activities of clinical trial data management including CRF design, database and edit check development, query generation/processing, reconciliation of CRF and electronic data, and database cleaning activities.
  • Assist in the planning and implementation of the data management portions of clinical research projects. Develops systems for organizing data to analyze, identify and report trends.
  • Work with CRAs and statistical department to provide accurate data acquisition and to furnish accurate and well-documented study databases to the statistical and clinical teams.
  • Responsible for timely identification of problems or issues that could affect the results or timely completion of the trial, or any protocol deviations, and for suggesting mechanisms for solving the problem.

The Essential Requirements Of The Job Include

 

  • Bachelor’s degree in scientific field or equivalent work experience
  • 2+ years clinical data management experience supporting clinical trials in a pharmaceutical, medical device, or biotech company.
  • Proven experience in working in relevant databases
  • Fluent level of English

It would be a plus if you also possess previous experience in:

 

  • General knowledge of FDA regulations.
  • Experience with web-based Electronic Data Capture (EDC) systems.
  • Good understanding of medical terminology, human physiology and laboratory testing preferred.

Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

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