Biology, Biotech and Pharmaceutical, Clinical Data, Clinical Laboratory, Clinical Outcomes, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Contract Research Organization (CRO), Cross-Functional, Customer Relations, Laboratory Testing, Multitasking, Organizational Skills, Plan Meetings, Project Development, Project Execution, Project Planning, Project Tracking, Project/Program Coordination, Project/Program Management, Risk Analysis, Team Player, Test Lab, Time Management
Our client, a world
leader in diagnostics and life sciences, is looking for a “Clinical
Science Program Specialist (100% Remote)".<\/b><\/span>
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Job Duration: Long
Term Contract (Possibility Of Extension)<\/span><\/b>
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Pay Rate : $35/hr on W2<\/span><\/b>
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Company Benefits:<\/span><\/b> Medical, Dental,
Vision, Paid Sick leave, 401K<\/span>
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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.<\/span>
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Key Responsibilities:<\/span><\/b>
<\/p>- Manage
multiple clinical testing and lab services projects under the guidance of
the Program Manager.<\/span>
<\/li> - Develop
project plans, timelines, and coordinate cross -functional activities to
ensure on -time execution.<\/span>
<\/li> - Monitor
project progress, identify risks and bottlenecks, and implement solutions
to maintain milestones.<\/span>
<\/li> - Oversee
sample processing workflows and ensure accurate reporting of results.<\/span>
<\/li> - Serve
as the primary liaison for pharmaceutical clients, CROs, site
investigators, and internal stakeholders.<\/span>
<\/li> - Coordinate
meetings, prepare agendas, document minutes, and communicate project
updates.<\/span>
<\/li> - Track
and maintain project reports and clinical study data.<\/span>
<\/li> - Promote
best practices and continuous improvement across clinical operations.<\/span>
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Qualifications:<\/span><\/b>
<\/p>- Bachelor’s
degree required; Life Sciences preferred.<\/span>
<\/li> - 2+
years of project coordination, clinical trial coordination, or project
management experience in the CRO, diagnostics, pharmaceutical, or
regulated industry.<\/span>
<\/li> - Exposure
to clinical studies and regulated documentation.<\/span>
<\/li> - Strong
organizational, communication, and collaboration skills.<\/span>
<\/li> - Ability
to manage multiple projects in a fast -paced environment.<\/span>
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Preferred
Qualifications:<\/span><\/b>
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