Principal Clinical Data Manager Job at cGxPServe, Madison, WI

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  • cGxPServe
  • Madison, WI

Job Description

Responsibilities:
  • Serve as lead CDM on assigned clinical trials by attending internal and external clinical trial project team meetings.
  • Responsible for the study-specific data management tasks from protocol review to database lock to ensure data are collected, reviewed, and delivered with high quality, on-time, and within scope.
  • Responsible for the accurate development of CRFs and edit specification per protocol and the completeness of user acceptance testing of CRFs and associated edit specifications for assigned clinical trials.
  • Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer documents including import/export agreements and data specifications.
  • Provide ad-hoc report development, and support database lock and archiving activities.
  • Review and contribute as a member of the CRF development team to develop the data collection modules on assigned studies where protocol requirements are outside of standard CRF library versions.
  • Ensure that medical coding is completed in a timely fashion, completed for all data cuts, and reviewed and approved by medical monitors.
  • Participate in the development of standard operating procedures (SOPs).
  • Mentor junior staff on clinical data management activities and procedures.
  • Provide guidance to clinical data management personnel on assigned projects, reviewing study documents as needed, e.g. Data Management Plan, Operational Plan for database locks.
  • Ensure project documentation is being archived in a timely manner into the Trial Master File.
  • Independently monitor own activities and project status for successful project deliverables according to timelines.
  • May lead or participate in initiatives to streamline data management processes.
Requirements:
  • Experience in clinical data management for 7+years.
  • Experience in vendor management of outsourced studies.
  • Demonstrate strong medical terminology skills.
  • Experience defining, entering, processing, reviewing, and validating clinical data; and understanding and following clinical trial protocols and data collection documents.
  • Medidata Rave experience required.
  • Medidata Suite products (Safety Gateway, ePRO, RTSM) preferred.
  • Experience with CDASH terminology and/or MedDRA and Who Drug medical coding preferred.
  • Possess effective written and verbal communication skills, interact professionally with personnel at all levels within and external to the company, and be dependable and a team player.
  • Demonstrate initiative, sound judgment and flexibility; possess effective time management and organizational skills; and be capable of working under deadlines.
  • Capable of working on multiple projects simultaneously, independently manage responsibilities according to deadlines, and define tracking tools to manage projects.
  • Experience in solving extremely complex and increasingly difficult problems, taking appropriate corrective action, and identify and implement improvements.
  • Possess a thorough knowledge of Data Management SOPs and regulatory requirements and be capable of providing guidance to and training peers.

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