Clinical Scientist Consultant – Neurology SME

Job not on LinkedIn

🔥 0 minutes ago

🏄 California – Remote

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💵 $103 / hour

⏱ Part Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 24%

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Logo of DAWAR CONSULTING INC

DAWAR CONSULTING INC

51 - 200 employees

Founded 2009

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

DAWAR CONSULTING INC. is a trusted provider of workforce solutions and professional services tailored for the Medical Science industry. Specializing in Human Capital Management (HCM) and ITSM consulting, DAWAR offers expert implementation of SaaS and Cloud-based solutions from platforms like Workday and ServiceNow. Their comprehensive staffing services include global talent acquisition, recruitment process outsourcing, and staff augmentation, ensuring that they connect skilled professionals with career opportunities while enhancing organizational productivity and efficiency.

📋 Description

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

🏖️ Benefits

• Medical • Paid Sick leave • 401K

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