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Health Education Jobs in Tucson, AZ

Clinical Science Program Specialist

IT Engagements

Tucson, AZ

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JOB DETAILS
SALARY
$35–$35
SKILLS
Best Practices, Biology, Biotech and Pharmaceutical, Clinical Data, Clinical Laboratory, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Continuous Improvement, 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
POSTED
2 days ago
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
Satya@Itengagements.com

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