Senior Clinical Scientist - First-In-Human Trials

black.ai

San Francisco (CA)

On-site

USD 140,000 - 210,000

Full time

14 days+
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Benefits offered by this job

Competitive salary
Share options
Daily meals provided
Professional development and training
Flexible hours and travel

Job summary

Coherence Neuro is seeking a Senior Clinical Scientist to provide scientific leadership for First In Human and Early Feasibility trials in a fast-paced neurotech startup. You will design studies, interpret data, and communicate findings to multidisciplinary teams across translational science, data, regulatory and quality groups.

The role focuses on patient safety, protocol execution, and collaboration with investigators and CROs to ensure rigorous, high-quality trials across geographies

Qualifications

  • Significant clinical-development experience in biotech/pharma/CRO/academic settings.
  • Experience supporting interventional trials from protocol to reporting.
  • Strong understanding of trial design, endpoints, data interpretation, and ICH-GCP.

Responsibilities

  • Provide day-to-day scientific leadership for ongoing intraoperative FIH study.
  • Lead protocol development, amendments, and related clinical documents.
  • Translate objectives into endpoints, criteria, assessments and data needs.
  • Review data to identify trends, risks, and data-quality issues.
  • Collaborate with CROs, regulatory, data science, and medical teams.
  • Contribute to regulatory submissions, abstracts, manuscripts, and reports.
  • Mentor colleagues and strengthen clinical-science practices.

Education

Advanced life sciences degree
Clinical trial leadership
ICH-GCP understanding
Scientific writing & communication
Cross-functional collaboration

Tools

Regulatory submissions

Job description

Coherence Neuro is seeking a Senior Clinical Scientist to provide scientific leadership for First In Human and Early Feasibility trials in a fast-paced neurotech startup. You will design studies, interpret data, and communicate findings to multidisciplinary teams across translational science, data, regulatory and quality groups.

The role focuses on patient safety, protocol execution, and collaboration with investigators and CROs to ensure rigorous, high-quality trials across geographies

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