Clinical Science Program Specialist; Remote Job Gilbert Arizona USA,Healthcare

Position: 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 with in the diagnostics or pharmaceutical industry.