Responsibilities
Core (all levels):
- Contribute to the design, execution, and interpretation of early clinical and clinical pharmacology studies
- Collaborate cross-functionally with Clinical Operations, Translational Sciences, Quantitative Clinical Pharmacology, and Statistics
- Support development of protocols, study reports, and regulatory submissions
- Analyze and interpret clinical safety and efficacy data with Medical and Scientific teams
- Monitor competitive landscape and emerging standards of care
- Ensure adherence to timelines, budgets, SOPs, and regulatory requirements
- Present data internally and contribute to external scientific communications
Additional by level:
- Associate Director: Lead components of studies; draft/own sections of clinical/regulatory documents; execute deliverables; present findings
- Director/Senior Director: Lead studies; drive cross-functional execution; contribute to strategy; serve as scientific leader; mentor juniors
- Executive Director: Provide strategic leadership across programs/areas; shape clinical development strategy and represent to governance; influence portfolio decisions and collaborations; act as subject matter expert; lead high-visibility initiatives
Qualifications
Minimum:
- PhD/PharmD/MD with 5+ years, OR BS/MS with 10+ years relevant experience
- Experience in early clinical development, clinical pharmacology, or related discipline
- Strong analytical, communication, and problem-solving skills; ability to work independently and collaboratively
Preferred (all levels):
- Experience in clinical pharmacology, immunology, or oncology
- Scientific curiosity/proactive mindset; ability to clearly present complex data