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

[email protected]/[email protected]