Clinical Science Program Specialist (100% Remote)

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 /