Clinical Scientist

Stevenson Search Partners

Santa Rosa, CAFull-timePosted Apr 9, 2026

Behavioral Health Market Context

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Job Description

ead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights that move programs forward.

Responsibilities:
• Lead design and execute clinical deliverables to support the CDP, including INDs, protocols, IBs, and study documents (CRFs, SAPs, data listings).
• Oversee clinical data generation, validation, and review, including query resolution, patient eligibility, and protocol deviation management.
• Perform study subject-level data analysis to inform clinical development strategy and reporting.
• Partner with medical teams, advisors, and Health Authorities, including support for HA/IRB interactions and responses.
• Contribute to therapeutic area research, KOL/investigator engagement, and development of scalable clinical processes.

Qualifications:
• A minimum of 8 years of relevant experience and an advanced degree (PharmD, PhD, MD, MSN, PA, MPH, etc.)
• Strong background in small molecule therapies and oncology clinical development.
• Experience in hematology required.
• Experience in early phase clinical trials required.

Qualifications

  • A minimum of 8 years of relevant experience and an advanced degree (PharmD, PhD, MD, MSN, PA, MPH, etc.)
  • Strong background in small molecule therapies and oncology clinical development
  • Experience in hematology required
  • Experience in early phase clinical trials required

Benefits

    Responsibilities

    • Summary: The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights that move programs forward
    • Lead design and execute clinical deliverables to support the CDP, including INDs, protocols, IBs, and study documents (CRFs, SAPs, data listings)
    • Oversee clinical data generation, validation, and review, including query resolution, patient eligibility, and protocol deviation management
    • Perform study subject-level data analysis to inform clinical development strategy and reporting
    • Partner with medical teams, advisors, and Health Authorities, including support for HA/IRB interactions and responses
    • Contribute to therapeutic area research, KOL/investigator engagement, and development of scalable clinical processes


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