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Sr. Clinical Data Manger
Sr. Clinical Data MangerKatalyst HealthCares & Life Sciences • Chicago, IL
Sr. Clinical Data Manger

Sr. Clinical Data Manger

Katalyst HealthCares & Life Sciences • Chicago, IL
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Responsibilities :

  • Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close.
  • This includes the EDC build and user acceptance testing (UAT), study data cleaning and reconciliation, query issue and resolution, and database locks.
  • They will ensure optimized data collection, flow and access across EDC and non-EDC data sources.
  • They are also responsible for accuracy, consistency, completeness and CDISC compliance of all clinical databases.
  • The role will operate as a key member of the Clinical Operations team.
  • Develop and maintain all data management documentation, including case report forms, data management plans, edit check specifications, data review plans and data transfer agreements.
  • Design case report forms (CRFs) for electronic data capture (EDC) systems for data collection.
  • Perform data entry and cleaning activities, including discrepancy management and query resolution.
  • Conduct data validation checks and implement quality control measures to ensure accuracy and completeness.
  • Collaborate with study team members to resolve data-related issues and discrepancies.
  • Generate and review data listings, summaries and reports for data review.
  • Serve as a primary or backup resource for issues about data management.
  • Ensure compliance with guidelines, Good Clinical Practice (GCP), CDISC standards and other relevant regulations.
  • Contribute to the development and validation of data management software tools.

Requirements :

  • BSc or MSc in Life Sciences, Data / Computer Science, Bioinformatics or equivalent industry experience.
  • years of data management experience in the pharmaceutical or biotechnology industries.
  • Strong expertise in project / program management including stakeholder management.
  • Knowledge of industry standards (CDISC, SDTM, CDASH).
  • In-depth understanding of Data Management regulatory guidelines : ICH, GCDMP, CFR Part .
  • Proven ability to pre-emptively identify data and system issues and mitigate risks to data quality.
  • Knowledge and experience with development, validation, execution, maintenance, documentation, and archival of clinical data.
  • Experience in development and implementation of Clinical data management standards and procedures.
  • Experience with web-based EDC, clinical data management systems and medical coding dictionaries such as MedDRA and WHO Drug.
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