Pathos AI
Medical Director, Clinical Development, Oncology
New York City, NY · Director
Sponsorship not specifiedDetected 55 days ago
GCPRESTAgentic AIExperimental DesignLeadershipMentoring
About the role
- You will work closely with R&D, Translational Medicine, Biomarker, and other internal teams to embed the right biomarker studies into every protocol and to correlate clinical and translational findings into the next development decision.
- This role sits at the intersection of deep oncology medicine and an AI native operating model.
Responsibilities
- Support executional delivery from site activation through enrollment to closeout, working in concert with Clinical Operations and AI agents that absorb status tracking, document version control, and coordination tasks.
- If you have spent your career building and shipping AI systems at scale, this is the environment where that experience becomes a superpower.
- You will report to the Chief Development Lead.
Requirements
- MD required, or US equivalent.
- 2 or more years of biotech or pharma industry experience in oncology clinical trial development and execution, preferably in solid tumors across Phase I, II, and III.
- Track record of delivering effective clinical trial plans and protocols within the drug development process.
- Ability to travel up to 30%, domestic and international.
- Experience designing biomarker driven trials and partnering closely with Translational Medicine and Biomarker teams.
- Fulfill GCP and compliance obligations, maintaining required training and audit-ready trial conduct.
Nice to have
- Direct experience with patient selection strategies grounded in molecular or computational evidence.
- Prior leadership of cross functional asset teams from candidate selection through clinical readout.
Benefits
- About the Role The Medical Director is a member of the Clinical Development team, accountable for the design, execution, oversight, and analysis of Pathos clinical trials.
- You will partner daily with each asset team to shape clinical strategy and provide medical and scientific judgment to the rest of the company as a working leader.
- Own medical monitoring and patient safety Lead medical review of trial data, including ongoing eligibility, protocol deviations, and safety signals.
- Assess key safety-related serious adverse events, approve safety narratives, and direct site education on safety management.
- Serve as the medical point of contact for clinical sites, addressing investigator questions and supporting enrollment quality.
- Execute trials with discipline Provide oversight and medical accountability across active studies.
- Adjudicate protocol violations, validate medical data, and serve as the medical resource for site staff.
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This listing is sourced directly from Pathos AI's careers page and normalized into a canonical job model.