Clinical Scientist Consultant / Neurology SME (100% Remote)” – Part time

Our client, a world leader in biotechnology and life sciences, is looking for a “Clinical Scientist Consultant / Neurology SME (100% Remote)” – Part time.

Job Duration: Long Term Contract (Possibility Of Extension)

Pay Rate : $103/hr on W2

Company Benefits: Medical, Paid Sick leave, 401K

We are seeking a Clinical Scientist Consultant / Neurology SME to provide scientific and clinical expertise supporting the planning and execution of pivotal neurology clinical programs.

Key Responsibilities

• Provide clinical SME guidance for neurology clinical trials, including pivotal studies.
  
• Review and provide input on protocols, endpoints, adjudication charters, endpoint assessment manuals, and clinical study plans.
  
• Identify clinical trial risks, operational gaps, enrollment challenges, data-quality concerns, and protocol issues and recommend mitigation strategies.
  
• Assess site performance, patient enrollment/retention, monitoring, vendor oversight, and overall study execution.
  
• Review clinical trial data, including protocol deviations, missing data, emerging trends, and data-quality issues.
  
• Partner cross-functionally with Clinical Development, Clinical Operations, Biometrics, Regulatory, Safety, and external vendors.
  
• Support pivotal-study and regulatory readiness activities.
  

Required Qualifications

• Strong experience in neurology clinical trials, preferably pivotal Phase 2/3 studies.
  
• Senior-level experience as a Clinical Scientist, Clinical Development Scientist/Lead, or similar clinical development role.
  
• Hands-on experience with protocol development/review, clinical endpoints, and clinical trial data.
  
• Ability to assess study risks and provide scientifically sound recommendations and mitigation strategies.
  
• Understanding of clinical trial operations, including sites, enrollment, monitoring, vendors, and data quality.
  

Preferred

• CIDP (Chronic Inflammatory Demyelinating Polyneuropathy) or related neuromuscular/neurology experience.
  
• Experience with endpoint adjudication.
  
• Regulatory submission/readiness experience.
  
• Experience supporting cross-functional pivotal clinical programs.
  

If interested, please send us your updated resume at

hr@dawarconsulting.com

akansha@dawarconsulting.com

Skills:
Adjudication, Biology, Biometrics, Biotech and Pharmaceutical, Clinical Data, Clinical Practices/Protocols, Clinical Research, Clinical Support, Clinical Trial, Consulting, Cross-Functional, Data Quality, Drug Development, Functional Programming Languages, Neurology, Neuromuscular, Performance Analysis, Regulations, Regulatory Submissions, Risk Analysis, Site Evaluation, Trend Analysis

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Dawar Consulting, Inc.