Clinical Science Program Specialist (100% Remote)

Dawar Consulting

  • Tucson, Arizona
  • 30+ days ago
  • Remote

    Highlights

    Drive cross-functional project execution, oversee sample workflow activities, and ensure timely, accurate delivery of clinical study results in a regulated environment. Coordinate and manage multiple clinical testing and laboratory services projects from initiation through completion, serving as the primary point of contact for pharmaceutical clients.

    Numbers & Facts

    LocationTucson, Arizona (
    Remote
    )
    Websitewww.dawarconsulting.com

    Description

    Our client, a world leader in diagnostics and life sciences, is looking for a “Clinical Science Program Specialist (100% Remote)".

     

    Job Duration: Long Term Contract (Possibility Of Extension)

    Pay Rate : $35/hr on W2

     

    Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

     

    Coordinate and manage multiple clinical testing and laboratory services projects from initiation through completion, serving as the primary point of contact for pharmaceutical clients. Drive cross-functional project execution, oversee sample workflow activities, and ensure timely, accurate delivery of clinical study results in a regulated environment.

     

    Key Responsibilities:

    • Manage multiple clinical testing and lab services projects under the guidance of the Program Manager.
    • Develop project plans, timelines, and coordinate cross-functional activities to ensure on-time execution.
    • Monitor project progress, identify risks and bottlenecks, and implement solutions to maintain milestones.
    • Oversee sample processing workflows and ensure accurate reporting of results.
    • Serve as the primary liaison for pharmaceutical clients, CROs, site investigators, and internal stakeholders.
    • Coordinate meetings, prepare agendas, document minutes, and communicate project updates.
    • Track and maintain project reports and clinical study data.
    • Promote best practices and continuous improvement across clinical operations.

     

    Qualifications:

    • Bachelor’s degree required; Life Sciences preferred.
    • 2+ years of project coordination, clinical trial coordination, or project management experience in the CRO, diagnostics, pharmaceutical, or regulated industry.
    • Exposure to clinical studies and regulated documentation.
    • Strong organizational, communication, and collaboration skills.
    • Ability to manage multiple projects in a fast-paced environment.

     

    Preferred Qualifications:

    • Experience with companion diagnostics (CDx), clinical testing, or biosample management.
    • Knowledge of clinical trial management processes and PMI methodologies.
    • Experience within the diagnostics or pharmaceutical industry.

     

     

     

    If interested, please send us your updated resume at

    hr@dawarconsulting.com

    /

    akansha@dawarconsulting.com


     

     



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