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Job description
About The Role
This is a strategic, senior-level physician-scientist role, owning late-stage oncology development programs end-to-end - from clinical strategy through regulatory submission. The team needs someone who can set direction, lead cross-functional teams, and engage Health Authorities with confidence not a pure study executor. Late-stage (Phase 2/3) program leadership is the top priority for this opening.
About The Role
This is a strategic, senior-level physician-scientist role, owning late-stage oncology development programs end-to-end - from clinical strategy through regulatory submission. The team needs someone who can set direction, lead cross-functional teams, and engage Health Authorities with confidence not a pure study executor. Late-stage (Phase 2/3) program leadership is the top priority for this opening.
What You'll Do
Own a Clinical Development Plan (CDP) as the responsible clinical lead for a program - not just execute studies
Lead or support studies across the full Phase 1-3 development continuum, with a focus on late-stage programs
Prepare for and present to Health Authorities (FDA/EMA)
Coordinate resources and provide strategic direction across a program, including managing junior team members
Interpret and apply translational/biomarker data to development decisions
Mentor junior Medical Directors and help shape team culture
What You'll Bring
MD required (Mandatory)
Strong oncology expertise, ideally solid tumors; hematology a plus
Minimum 5 years' industry clinical R&D experience at pharma/biotech
Experience leading or supporting studies across the full Phase 1-3 continuum
Demonstrated contribution to registration-enabling activities and Health Authority interactions
Ability to work across global, matrixed teams
ICH-GCP/FDA/EMA regulatory fluency
End-to-end development experience in a big biotech / big pharma environment
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.