Associate Scientist, Clinical Development
Core
Supports clinical development in early and late phases through registration by informing study design, overseeing execution, maintaining databases, and analyzing data.
Role type
Associate Scientist, Clinical Development
Builds
Clinical trial programs and regulatory filings for neurological, psychiatric, endocrine, and immunological disorders
Domain
Biopharmaceuticals / Clinical Development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial methodology, data analysis, regulatory document preparation, study design input, outcome measure development, literature research, site monitoring, ICH-GCP knowledge
Preferred skills
Strategic thinking, project management, external collaboration, competitor landscape analysis
Technologies
Clinical databases, statistical analysis tools, regulatory filing systems
Responsibilities
Provide clinical support and scientific opinion to study teams; Contribute to study design, protocol concepts, and statistical analysis plans; Monitor patient data and site adherence to protocol; Prepare abstracts, manuscripts, and clinical sections of regulatory documents; Collaborate with internal clinicians and external opinion leaders
Seniority
Mid-level, hands-on IC
