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Lead Clinical Data Manager

Last updated: 2026/02/19 at 6:35 PM
By
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3 Min Read
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  • Permanent
  • United States
  • Posted 3 weeks ago
Karwell Technologies

Website Karwell Technologies

Karwell Technologies

Company : Karwell Technologies

Responsibilities:

  • Lead the data quality evaluation by investigating all clinical and operational data, evaluating trends, deviations, using visual analytics tools and ad hoc reports.
  • Manage high complex studies and support specific activities of studies managed by other data managers or consultants.
  • Provide technical tutoring and supervise data managers and/or contractors assigned to clinical studies by conducting regular reviews of activity status.
  • In-depth knowledge of Clinical Data Interchange Standards Consortium (CDISC) relating to data standards including Study Data Tabulation Model (SDTM) and Case Report Tabulation Data Definition Specification (Define.xml).
  • Manage and guide providers, setting requirements, preparing or reviewing Request for Proposals and monitoring performance.
  • Regularly monitor data management costs of the assigned studies ensuring respect of budget.
  • Define and proactively manage risks with potential impact on study systems setup, study conduction, or reliability of study results.
  • Ensure all data collection systems for assigned projects are setup, tested and fit for purpose according to expectations and timelines.
  • Define the strategy and lead the preparation of data package for regulatory submission.
  • Represent data management for auditing and regulatory inspection.
  • EHR data, data collected directly from patients, omics data, other secondary data).
  • Advanced analytical and technical skills to interrogate and mine high volumes of data from a variety of sources.

Requirements:

  • Minimum 8+ years of experience in Clinical Data Management in CROs or Pharmaceutical Industry.
  • Solid knowledge of drug development processes.
  • Strong data management expertise.
  • Excellent knowledge of Good Clinical Data practices, GCP and regulatory requirements.
  • Experience with clinical databases, electronic data capture (EDC) systems, wearables, and sensors to collect data directly from patients.
  • Excellent knowledge of Risk-Based approach.
  • Knowledge of Real-World data sources and processes to collect/manage different types of sources.
  • Basic knowledge of Artificial Intelligence (AI).
  • Project Management skills.
  • Excellence in planning and priorities setting.
  • Analytical, problem-solving skills and ability to take ownership of decision-making.
  • Strong commitment to quality.
  • Excellent oral and written communication and presentation skills.
  • Ability to collaborate and work in a team-based environment.
  • Courage, resilience, and ability to adjust to a rapidly changing environment.
  • Experience with Medidata platform.
  • Familiarity with other platforms for secondary data.
  • Proficiency in SAS System.

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