IT ENGAGEMENTS, INC.
IT ENGAGEMENTS, INC.

Clinical Science Program Specialist

Tucson, AZ, US • Posted 1 day ago • Updated 1 day ago
Contract W2
On-site
Fitment

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Job Details

Skills

  • Clinical Science
  • clinical testing

Summary

Greetings from IT Engagements
IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients.
Job Summary
Job Title: Clinical Science Program Specialist
Work Location: 1910 East Innovation Park Drive, Tucson, AZ USA - 85755
The Opportunity
  • Manages multiple clinical testing and lab services projects from initiation through contract completion under
    supervision of Program Manager. Acts as primary point of contact to Pharma customers.
  • Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and:
    - Develops project plans, establish and coordinates timelines for assigned projects and functions;
    - Manages execution of cross-functional plans and tracks progress of activities;
    - Identifies gaps, potential bottlenecks or delays and challenge assumptions.
  • Oversees and guides day to day activities of sample process flow and accurate reporting of results.
    Implements / pulls in best practices within the clinical sciences team; fosters continuous improvement by
    ensuring knowledge and experience exchange
  • Guides and manages cross-functional interactions to complete the assigned projects within the deadline.
  • Interfaces with resources outside of the company (Contract Research Organizations (CROs), site
    investigators, client counterparts, etc.) and serves as single point of contact with Pharma and Roche clients.
  • Manages meeting activities such as setting agendas, organizing meeting time and editing meeting minutes.
  • Tracks, maintains and communicates project reports and clinical study data to Pharma and Roche clients.
Requirements
  • At least 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation
  • Exposure to clinical studies
  • Experience with clinical projects that require rapid activity/milestone achievement.
  • Strong communication, collaboration, and organizational skills are required
  • Bachelor's degree is required (Life Sciences is preferred)
Preferred
  • Previous experience with standard project management process (PMI) desired.
  • Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow preferred.
  • Preferred experience in clinical studies or companion diagnostics
  • Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred.
Regards,
Satya
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91119149
  • Position Id: 2026-2289
  • Posted 1 day ago
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