Clinical Science Program Specialist (100% Remote)

United StatesUnited States·Tucsonmid
OtherProgram Specialist
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Quick Summary

Key Responsibilities

Manage multiple clinical testing and lab services projects under the guidance of the Program Manager. Develop project plans, timelines,

Requirements Summary

Bachelor’s degree required; Life Sciences preferred. 2+ years of project coordination, clinical trial coordination, or project management experience in the CRO, diagnostics, pharmaceutical,

Technical Tools
OtherProgram Specialist
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

Location & Eligibility

Where is the job
Tucson, United States
On-site at the office

Listing Details

Posted
June 23, 2026
First seen
September 27, 2026
Last seen
September 27, 2026

Posting Health

Days active
-1
Repost count
0
Trust Level
14%
Scored at
September 27, 2026

Signal breakdown

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dawarconsultingClinical Science Program Specialist (100% Remote)