Clinical Scientist Consultant / Neurology SME (100% Remote)” – Part time
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.
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, pleasesend us your updated resume at
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