Clinical Science Program Specialist (100% Remote)

🏢 Dawar Consulting, Inc. · all Dawar Consulting, Inc. jobs
📍 United States
📅 Posted 2026-08-24 · via Himalayas
🏷 Clinical-Project-Coordination,Clinical-Trial-Management,Laboratory-Services,Clinical-Science,Clinical-Programs-Specialist,Clinical-Science-Specialist,Clinical-Program-Manager,Pharmaceutical
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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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