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Revolution Medicines

Senior Director, Patient Reported Outcomes

Revolution Medicines · Remote (United States)

Posted 22 days ago

or apply directly on Revolution Medicines's site. We never take the application ourselves.

Is this posting real?

This role has been open
22 days
Revolution Medicines's roles stay open a median of 43 days
Reposted
No
Salary listed
No
0% of Revolution Medicines's roles list one
Ghost-job risk at Revolution Medicines
low
0 stale, 6 reposted of 264 open
Hiring momentum
449 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-09-17

Measured from postings appearing on and disappearing from Revolution Medicines's own greenhouse board since 2026-08-03. Full hiring picture for Revolution Medicines.

About this role

The Senior Director, Patient Reported Outcomes (PRO) will lead the development and execution of PRO strategies for clinical development programs at Revolution Medicines. This role involves collaborating with cross-functional teams to integrate patient-centered outcomes into study designs and regulatory submissions, while also providing methodological guidance and managing research activities. Initially an individual contributor position, there is potential for future people-management responsibilities as the organization expands.

Our read on this posting3.0out of 5
benefits
3/5
freshness
4/5
career value
4/5
role clarity
4/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Revolution Medicines as an employer.

What you need

  • Advanced degree (eg, Ph.D., Sc.D., Dr.P.H., Psy.D., M.D., Pharm.D., M.P.H., M.S., or equivalent) in psychology, psychometrics, epidemiology, public health, health outcomes research, behavioral science, or a related discipline
  • Minimum of 13 years of relevant experience in patient-reported outcomes, patient-focused drug development, health outcomes research, or a related field
  • Experience developing and implementing PRO strategies for clinical development programs, preferably including late-stage studies and support for regulatory interactions or submissions
  • Strong expertise in qualitative and quantitative PRO methodologies
  • Working knowledge of global regulatory expectations related to patient-focused drug development and clinical outcome assessments
  • Ability to work effectively in cross-functional teams and manage multiple priorities

Nice to have

  • Experience developing or implementing PRO strategy in oncology clinical development
  • Experience supporting Phase 2 and/or Phase 3 development programs
  • Experience working with external research vendors, consultants, academic collaborators, patient organizations, or other partners involved in patient-centered outcomes research
  • Experience contributing to regulatory or HTA interactions, scientific publications, or cross-functional capability-building activities related to PROs

What you get

  • Base pay salary range of $232,000 — $290,000 USD
  • Competitive cash compensation
  • Robust equity awards
  • Strong benefits
  • Significant learning and development opportunities

Worth weighing

  • No specific mention of remote work flexibility beyond the stated remote location
  • The role is initially an individual contributor position with future management potential, which may appeal to candidates looking for growth
  • Salary range is provided for onsite work in Redwood City, CA, and will be adjusted based on local market for remote candidates

Summarised from Revolution Medicines's posting. Read the full original.

Listed by Revolution Medicines on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

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