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Title:Sr Clinical Data Coordinator
Location:CA - South San Francisco

Maintain a project-level perspective on data management issues, activities and deliverables (i.e. reviewing protocols for cross-project consistency, identifying project-level standard eCRF modules, coordinating data management activities across protocols to meet overall project deadlines and objectives).

  • Manage projects resourced externally via contract research organizations or corporate partners.
  • Provide early strategic input into protocol design focused on data management issues.
  • Lead the development of eCRFs and database specifications by interacting with other functional area representatives.
  • Review and resolve data discrepancies via standardized reports and close interaction with project clinical research professionals.
  • Interact regularly with Clinical Data Management groups to ensure that project objectives are understood and met.
  • Develop and execute ad hoc database queries using relational database tools.
  • Participate in departmental discussion groups, formal working groups or special projects.

  • Requires a B.A./B.S. with a minimum of 3-4 years experience in Clinical Data Management.
  • Knowledge of core clinical data management applications (Unix, MS Word, web browser, relational database, query tools).
  • Clinical data management system experience (EDC Medidata RAVE preferred).
  • Good understanding of the role of data management, biostatistics and statistical programming in the drug development process.
  • Understanding of the conceptual basis for data management conventions, standards and processes.
  • Ability to multi-task and effectively set own priorities.
  • Good organizational skills.
  • Strong communication and interpersonal skills.

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