Salary
💰 $226,300 - $377,100 per year
About the role
- Support PD-1/VEGF bispecific program and late stage clinical trial(s) as an individual contributor
- Provide clinical leadership across 2-3 study teams in collaboration with Clinical Scientists
- Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring
- Lead peer-to-peer interactions with investigators and serve as point of contact for clinical issues
- Coordinate clinical issues between study team, investigators, ethics committees, steering committees, and regulatory authorities
- Lead and contribute to development and maintenance of clinical trial and regulatory documents with cross-functional team
- Collaborate with Clinical Scientist to review and interpret clinical data, identify key findings and implications, and communicate to stakeholders
- Maintain clinical expertise by staying abreast of latest developments, literature, and guidelines to advise on clinical development plans
Requirements
- Medical degree with relevant clinical or industry experience considered (typically 4+ years)
- 2-5 years industry experience
- Prior experience in clinical trials and supporting development programs
- Board certified/eligible in oncology or equivalent (preferred)
- Demonstrated leadership: ability to influence and collaborate with peers, develop and coach others, oversee and guide colleagues
- Experience with medical monitoring activities including eligibility assessment, data review and safety monitoring
- Experience in peer-to-peer interactions with investigators and interactions with ethics committees, steering committees, and regulatory authorities
- Experience in development and maintenance of clinical trial and regulatory documents
- Permanent work authorization in the United States required