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

Role Summary

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

• Job Duration: LongTerm Contract (Possibility Of Extension)
• Pay Rate: $103/hr onW2
• Company Benefits: Medical, Paid Sickleave, 401K

We are seeking a ClinicalScientist Consultant / Neurology SME to provide scientific and clinicalexpertise supporting the planning and execution of pivotal neurology clinicalprograms.

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.

Requirements

• 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, pleasesend us your updated resume at
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