Lead protocol development and optimize clinical trial designs to assess investigational oncology drugs effectively
Collaborate with cross-functional teams to develop comprehensive clinical development plans aligned with program strategies
Drive execution of global clinical studies while ensuring adherence to protocols, regulatory standards, and ethical guidelines
Engage with internal and external scientific experts to interpret emerging data and incorporate best practices into trial conduct
Monitor study progress, review data trends, resolve adverse events, and ensure compliance throughout the study lifecycle
Mentor junior colleagues to cultivate a culture of continuous improvement within the clinical science team

Bachelor’s degree in life sciences or healthcare; advanced degree preferred with 8+ years of clinical experience
Proven experience in clinical development within oncology or immuno-oncology settings
Strong understanding of Good Clinical Practice (GCP) and all phases of drug development (Phase 1–3)
Proficiency in planning and executing global clinical trials within pharmaceutical companies or CROs
Collaborative mindset with proven ability to work effectively in matrix environments and influence stakeholders without direct authority
Skilled in analyzing clinical data using tools like EDC platforms or Excel; experience in process optimization is desirable

competitive remuneration packages based on the specific role and candidate’s qualifications and experience

Associate Director, Clinical Science

Key skills