Clinical Science Program Specialist (100% Remote

Tucson, United States | Posted on 06/23/2026

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 ofthe Program Manager.
• Develop project plans, timelines, and coordinate cross-functional activities toensure 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.
• Serveas the primary liaison for pharmaceutical clients, CROs, site investigators, and internal stakeholders.
• Coordinate meetings, prepare agendas, document minutes, and communicate project updates.
• Trackand maintain project reports and clinical study data.
• Promote best practices and continuous improvement across clinical operations.

Qualifications:

• Bachelor’sdegree 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.
• Abilityto manage multiple projects in a fast-paced environment.

Preferred Qualifications:

• Experience with companion diagnostics (CDx), clinical testing, or biosamplemanagement.
• Knowledge of clinical trial management processes and PMI methodologies.
• Experience within the diagnostics or pharmaceutical industry.

If interested, pleases end us your updated resume at