dawarconsulting3mo ago
Clinical Science Program Specialist (100% Remote)
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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External application
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