Associate Director, Clinical Scientist, Oncology
Core
Leads the development, evaluation, planning, and execution of clinical studies for oncology drug candidates, ensuring scientific integrity and data interpretation.
Role type
Senior IC clinical scientist with program leadership responsibilities
Builds
Global clinical development programs for early and late-stage oncology assets
Domain
Oncology / Pharmaceutical Clinical Development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical study design and execution, regulatory compliance (FDA/EMEA/ICH/GCP), medical monitoring plan authoring, clinical data review and safety monitoring, protocol development, cross-functional matrix leadership, strategic proposal development
Preferred skills
PhD/MD/PharmD/MSc in life science/healthcare, experience with Expanded Synopsis and Clinical Study Reports, mentoring junior team members
Technologies
None explicitly listed
Responsibilities
Lead clinical scientist for programs or delegate for Therapeutic area Lead, contribute to scientific advisory boards and study steering committees, author and review clinical trial protocols and amendments, present data to external investigators and internal stakeholders, perform clinical/medical data review and safety monitoring, design mitigation strategies for program objectives
Seniority
Senior, hands-on IC with program leadership
