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Clinical Science Program Specialist (100% Remote)

Dawar Consulting, Inc.
Posted a month ago, valid for a month
Location

San Vicente, AZ, US

Salary

$35 per hour

Contract type

Contract

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Sonic Summary

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  • Our client, a world leader in diagnostics and life sciences, is seeking a Clinical Science Program Specialist for a 100% remote position.
  • This long-term contract role offers a pay rate of $35 per hour on a W2 basis, along with benefits including medical, dental, vision, paid sick leave, and 401K.
  • The specialist will coordinate and manage multiple clinical testing and laboratory service projects, serving as the primary contact for pharmaceutical clients.
  • Candidates must have a Bachelor’s degree, preferably in Life Sciences, and at least 2 years of project coordination or management experience in a regulated industry.
  • Preferred qualifications include experience with companion diagnostics and knowledge of clinical trial management processes.

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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