Cynet Systems
Cynet Systems

Clinical Science Program Specialist

Tucson, AZ, US • Posted 1 day ago • Updated 1 day ago
Contract Corp To Corp
Contract W2
12 Months
On-site
Depends on Experience
Fitment

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Job Details

Skills

  • Clinical Science Program Specialist

Summary

We are looking for Clinical Science Program Specialist for our client in Tucson, AZ

Job Title: Clinical Science Program Specialist

Job Location: Tucson, AZ

Job Type: Contract

Job Overview:

Requirement/Must Have:

  • 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).

Responsibilities:

  • Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services.
  • Develops project plans, establishes 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 challenges assumptions.
  • Oversees and guides day to day activities of sample process flow and accurate reporting of results.
  • Implements 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 organization (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and 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 clients.

Nice to Have:

  • 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.
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: 10516350
  • Position Id: AZ_CSPT_0623
  • Posted 1 day ago
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