Sr. Director, Epidemiology & RWE Analytics

Scorpion Therapeutics

San Diego (CA)

On-site

USD 230,000 - 314,000

Full time

14 days+

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Benefits offered by this job

Base salary 230k–314k USD
Annual bonus target 35%
Equity long-term incentive eligibility
Retirement match
Paid time off
Caregiver/parental and medical leave
Medical/prescription/dental/vision

Job summary

Scorpion Therapeutics in San Diego seeks a senior leader to own enterprise epidemiology and real-world evidence strategy, governance, and execution across portfolios. You will partner with R&D, Medical, Market Access, and Analytics to shape globally relevant evidence programs and support regulatory submissions.

This role requires deep epidemiology expertise, proven leadership of cross-functional teams, and the ability to translate strategy into portfolio plans.

Qualifications

  • Master’s + 12+ years relevant experience OR PhD/PharmD/MD (Epidemiology/Public Health or related) + 10+ years pharma/biotech epidemiology/RWE experience OR previous management experience.
  • In-depth knowledge of clinical/regulatory evidence; trusted-advisor mindset.
  • Strong leadership, stakeholder management, communication, and analytical/judgment skills.

Responsibilities

  • Define and lead enterprise epidemiology/RWE strategy and align with cross-functional priorities.
  • Establish functional governance (methodological standards, evidence quality, prioritization, ways of working).
  • Translate enterprise strategy into portfolio/therapeutic-area evidence plans.
  • Advise executives on population health, disease epidemiology, and RWE.
  • Drive evidence for regulatory submissions, HTAs, reimbursement, and global value demonstration.
  • Lead/coach/develop staff; manage resourcing and budget.
  • Integrate RWE into Phase 3 design and late-stage development (e.g., external control arms, endpoint validation).
  • Ensure consistent, high-quality epidemiologic/observational methods; partner with DSPV for safety-focused analyses.
  • Collaborate with HEOR/Market Access; ensure outputs meet payer/HTA/regulatory expectations; represent function in scientific advice/discussions and engage external stakeholders.

Skills

Leadership
Stakeholder management
Communication
Analytical/judgment skills

Education

Master’s degree
PhD/PharmD/MD in Epidemiology/Public Health

Job description

About The Role
  • Provides senior leadership for enterprise-wide epidemiology and real-world evidence (RWE) strategy, governance, and execution across therapeutic areas and portfolios.
  • Accountable for defining and delivering fit-for-purpose, consistent evidence strategies supporting clinical development, regulatory submissions, medical affairs, and market access.
  • Serves as a senior thought partner to R&D, Medical, Market Access, and Analytics; leads teams responsible for externally facing epidemiologic and RWE programs.
Your Contributions (include, but are not limited to)
  • Define and lead enterprise epidemiology/RWE strategy and align with cross-functional priorities.
  • Establish functional governance (methodological standards, evidence quality, prioritization, ways of working).
  • Translate enterprise strategy into portfolio/therapeutic-area evidence plans.
  • Advise executives on population health, disease epidemiology, and RWE.
  • Drive evidence for regulatory submissions, HTAs, reimbursement, and global value demonstration.
  • Lead/coach/develop staff; manage resourcing and budget.
  • Integrate RWE into Phase 3 design and late-stage development (e.g., external control arms, endpoint validation).
  • Ensure consistent, high-quality epidemiologic/observational methods; partner with DSPV for safety-focused analyses.
  • Collaborate with HEOR/Market Access; ensure outputs meet payer/HTA/regulatory expectations; represent function in scientific advice/discussions and engage external stakeholders.
Requirements
  • Master’s + 12+ years relevant experience OR PhD/PharmD/MD (Epidemiology/Public Health or related) + 10+ years pharma/biotech epidemiology/RWE experience OR previous management experience.
  • In-depth knowledge of clinical/regulatory evidence; trusted-advisor mindset.
  • Strong leadership, stakeholder management, communication, and analytical/judgment skills.
  • Demonstrated leadership of enterprise evidence strategies and people leaders.
  • Deep understanding of regulatory, HTA, payer, and market access evidence requirements.
Compensation/Benefits (as stated)
  • Base salary: $230,100.00–$314,000.00; annual bonus target 35%; equity long-term incentive eligibility.
  • Retirement match, paid time off, caregiver/parental and medical leave, and medical/prescription/dental/vision coverage.
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