Senior Clinical Data Coordinator
Pra Health Sciences
Canada
4d ago

Responsibilities :

  • Serves as lead clinical data coordinator for one or more projects.
  • Maintains data management study documentation as appropriate.
  • Manages the data review and external data reconciliation process.
  • Mentors and trains multiple lead clinical data coordinators for successful study startup, maintenance, and closeout.
  • Supports and leads PRA data management initiatives to develop training for data management processes and systems.
  • May serve as an external representative of PRA for client and industry meetings.
  • Promotes a positive and professional work environment and may be asked to be a backup for the functional manager position.
  • May participate in sponsor and / or third-party audits.
  • Demonstrates strong knowledge of computerized information systems and standard application software (Windows, MS Office).
  • Exhibits strong understanding of clinical data management systems or electronic data capture software.
  • Exhibits advanced knowledge of clinical data management.
  • Displays excellent written and oral communication skills.
  • Shows expertise in all aspects of the life cycle of a data management study, from start-up to lock.
  • Acts as a subject matter expert (SME) for various technologies or processes.
  • Performs duties at a high standard with limited supervision.
  • Problems may require clarification. Uses basic analytical techniques. Uses previous experience to identify the most appropriate option or to adapt or improve existing approaches.
  • Resolves issues which are varied and non-routine. Provides functional management and project teams with solutions.

  • Interprets or explains data or information to deliver messages to audiences not knowledgeable about the subject matter.
  • Contributes to the achievement of goals through personal effort and influence over others in department. Impact is limited to achievement of short-
  • medium term achievement of goals.

    Requirements :

  • Bachelor’s degree desired.
  • 5 years of clinical data experience required.
  • Experience leading multiple studies at once from start-up to lock required.
  • To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.
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