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Senior Clinical Data Manager

Role overview

Qualifications

  • Minimum of four years of clinical data management experience
  • Hands-on data review experience
  • Demonstrated proficiency in Medidata Rave

Responsibilities

  • Provide comprehensive data management support for assigned clinical studies
  • Perform ongoing data review to ensure accuracy, completeness, and consistency of clinical trial data
  • Ensure compliance with the study protocol and data management plan

Key facts

Hard skills

About the company

Cytel logo

Cytel

  • Clinical Research (CRO)
  • Large
  • 1,001–5,000
Cytel Inc., an advanced analytics leader with over thirty years of experience providing sophisticated quantitative insights to executive decision-makers in the lifesciences. Cytel employs a range of data science tools from biostatistics to machine learning to help executives in the life-sciences to make confident decisions powered by data. We are probably best known for being leaders in the field of adaptive clinical trial design, a subset of trial design that uses interim looks to enhance the patient safety and commercial value of pharmaceutical products. We also have specialists in Bayesian statistics, real world evidence, artificial intelligence, health economics, and a number of other research fields to ensure that academic and scientific findings can have impact on industry quickly and seamlessly. www.cytel.com

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Job description

The Senior Clinical Data Manager will provide comprehensive data management support for assigned clinical studies. The SCDM will be responsible for performing ongoing data review to ensure accuracy, completeness, and consistency of clinical trial data in accordance with the study protocol and data management plan. The CDM will have a minimum of four years of clinical data management experience, including hands-on data review experience, and demonstrated proficiency in Medidata Rave.

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