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Health Education Jobs in Tucson, AZ

Clinical Science Program Specialist

Integrated Resources, Inc

Tucson, AZ(remote)

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JOB DETAILS
SALARY
SKILLS
Best Practices, Biology, Biotech and Pharmaceutical, Clinical Data, Clinical Laboratory, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Continuous Improvement, Contract Management, Contract Research Organization (CRO), Cross-Functional, Customer Relations, Documentation, Editing, Laboratory Testing, Meeting Minutes, Organizational Skills, Pharmaceutical Data, Plan Meetings, Process Flow, Project Development, Project Planning, Project Tracking, Project/Program Management, Team Player, Test Lab, Time Management
LOCATION
Tucson, AZ(remote)
POSTED
4 days ago
Job Title- Clinical Science Program Specialist
Location- Tucson, Client
Duration- 12 Months Contract
*** This is a requisition for several Clinical Science Program Specialists in CDx Pharma Services. The pay rate is $35/hr.

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, 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 challenge assumptions.
  • Overseas 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 manage cross-functional interactions to complete the assigned projects within the deadline.
  • Interfaces with resources outside of the Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and clients.
  • Manage 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 Client 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.

About the Company

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Integrated Resources, Inc

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