Sr. Director, Clinical Research-CVM Nephrology

Scorpion Therapeutics

Cambridge (MA)

Hybrid

USD 200,000 - 320,000

Full time

14 days+
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Benefits offered by this job

Hybrid work arrangement

Job summary

Scorpion Therapeutics is seeking a Senior Medical Director, Clinical Research for the CVM area, leading early kidney-focused RNAi programs. You will drive clinical strategy, advance first-in-human and proof-of-concept studies, and ensure operational excellence.

The role requires MD/MD-PhD with nephrology expertise and 5+ years in early-phase renal drug development, with cross-functional collaboration and external engagement key to success. Hybrid work located in Cambridge, MA.

Qualifications

  • MD or MD/PhD with nephrology specialization preferred.
  • 5+ years in early-phase CVM or renal drug development, including trial design.
  • Experience in regulatory interactions and program leadership.

Responsibilities

  • Provide clinical program leadership.
  • Oversee clinical trials and monitoring.
  • Ensure safety monitoring across programs.
  • Develop comprehensive clinical development plans (CDPs).
  • Collaborate with R&D, Regulatory, and Medical Affairs across functions.
  • Engage with external scientific communities and stakeholders.

Skills

Strategic planning
Scientific judgment
Medical monitoring
Governance navigation

Education

MD
MD/PhD
Board Certified in Nephrology

Job description

Role

Senior Medical Director, Clinical Research in CVM therapeutic area, leading early-stage kidney programs with a focus on RNAi therapeutics. Objectives include driving clinical strategy, advancing first-in-human and proof-of-concept studies, and ensuring operational excellence.

Responsibilities
  • clinical program leadership
  • trial oversight
  • safety monitoring
  • development of clinical development plans (CDPs)
  • cross-functional collaboration with R&D, Regulatory, and Medical Affairs
  • external scientific engagement
Qualifications

MD or MD/PhD, Board Certified or specialist training in Nephrology preferred; 5+ years industry experience in early-phase CVM or renal drug development, including trial design, regulatory interactions, and program leadership.

Skills
  • strategic planning
  • scientific judgment
  • medical monitoring
  • navigating internal governance
High-Value

focus on RNAi therapeutics in kidney disease, early clinical development, first-in-human trials, extensive cross-functional and external collaboration.

Work setup

hybrid at Cambridge, MA; travel not specified.

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