Associate Director, Clinical Scientist
Core
Lead clinical development programs for oncology therapies, managing strategy, study design, execution, and regulatory documentation from startup to report.
Role type
Senior IC clinical scientist (oncology)
Builds
Clinical development programs for cancer therapies
Domain
Biotechnology / Oncology
Required skills
Global clinical study design, drug development lifecycle, oncology therapeutic area, GCP/ICH guidelines, clinical trial data analysis, medical monitoring, stakeholder management, strategic planning, budget management, SOP development
Preferred skills
Key opinion leader network building, therapeutic area research, process improvement, cross-functional collaboration
Technologies
Clinical Development IT solutions, Word, PowerPoint, Excel
Responsibilities
Generate and review clinical/regulatory documents (protocols, reports, manuscripts); lead clinical study design and execution; provide scientific expertise for site/vendor selection; analyze clinical trial data; serve as medical monitor; present data internally and externally; build investigator networks; contribute to competitor analysis; optimize standards and processes; manage budget and resources.
Seniority
Senior, hands-on IC