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.
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.

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Originally posted on Himalayas

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.

Clinical Science Program Specialist (100% Remote)

Summary