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Clinical Science Program Specialist (100% Remote)

Dawar Consulting, Inc.

  • $35 / hour
  • United States
  • Contractor
  • 18 hours ago
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About the role

Our client, a worldleader in diagnostics and life sciences, is looking for a“ClinicalScience Program Specialist (100% Remote)".

Job Duration: LongTerm Contract (Possibility Of Extension)

Pay Rate : $35/hr on W2

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

Coordinate and managemultiple clinical testing and laboratory services projects from initiationthrough completion, serving as the primary point of contact for pharmaceuticalclients. Drive cross-functional project execution, oversee sample workflow activities,and ensure timely, accurate delivery of clinical study results in a regulatedenvironment.

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.

PreferredQualifications:

  • 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, pleasesend us your updated resume at

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Originally posted on Himalayas

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