Clinical Science Program Specialist (100% Remote)

Job Description

Job Description

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

[email protected]/[email protected]