Senior Director, Global Clinical Development & Strategy

Scorpion Therapeutics

Pennsylvania

On-site

USD 275,000 - 458,000

Full time

14 days+
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Benefits offered by this job

Base salary
Bonus target 25%
Long-term incentive
Health + 401(k)

Job summary

Scorpion Therapeutics is seeking an MD/DO leader to drive clinical development for internal medicine assets. You will lead a cross-functional Clinical Development Team to design, execute, and interpret studies for worldwide regulatory submissions.

The role includes developing the Clinical Development Plan, pediatric investigation plan, and submission deliverables; you will provide therapy area expertise and collaborate on statistical analysis, safety reviews, and regulatory disclosures.

Qualifications

  • MD or DO with 8+ years in clinical research/development.
  • Experience leading multi-disciplinary teams across discovery to submission.
  • Background in internal medicine, endocrinology, or weight management is preferred.

Responsibilities

  • Serve as single clinical point of accountability for clinical development of assigned assets.
  • Lead cross-functional Clinical Development Team to design, execute, and interpret studies for worldwide regulatory submissions.
  • Create and endorse the Clinical Development Plan and protocol designs; ensure trial feasibility and execution.
  • Lead pediatric investigation plan and protocol design; develop submission deliverables including IAP, IARP, TLFs.
  • Provide therapy area expertise and collaborate on statistical analysis plans and data disclosures.
  • Support regulatory submissions, safety disclosures, and product labeling maintenance.

Skills

Clinical development leadership
Regulatory affairs
Cross-functional collaboration
Pediatric development

Education

MD or DO

Job description

Scorpion Therapeutics is seeking an MD/DO leader to drive clinical development for internal medicine assets. You will lead a cross-functional Clinical Development Team to design, execute, and interpret studies for worldwide regulatory submissions.

The role includes developing the Clinical Development Plan, pediatric investigation plan, and submission deliverables; you will provide therapy area expertise and collaborate on statistical analysis, safety reviews, and regulatory disclosures.

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