Oncology Clinical Development Director (Hybrid)

Scorpion Therapeutics

Pennsylvania

Hybrid

USD 180,000 - 240,000

Full time

14 days+
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Benefits offered by this job

Relocation assistance

Job summary

Scorpion Therapeutics in the United States seeks a Medical Director to provide Clinical Development leadership for the PF 4404 program, overseeing design, conduct, and analysis of trials while coordinating with regulatory affairs, pharmacovigilance, biostatistics, and medical affairs.

You will support clinical operations, investigators, and external stakeholders to uphold scientific, ethical, and regulatory standards.

Qualifications

  • Primary medical degree and 4+ years of experience.
  • Licensed to prescribe medicines independently for at least 2 years.
  • Board certified/eligible in oncology (or equivalent) preferred.
  • Late-stage clinical development experience preferred.

Responsibilities

  • Provide clinical leadership across 2–3 study teams aligned to company objectives.
  • Conduct medical monitoring (eligibility assessment, data review, safety monitoring).
  • Lead peer-to-peer interactions with investigators.
  • Serve as point of contact for clinical issues between study team, investigators, ethics/steering committees, and regulatory authorities.
  • Lead and contribute to development and maintenance of clinical trial and regulatory documents with cross-functional team.
  • Review and interpret clinical data, identify key findings and implications for stakeholders.
  • Stay current on developments, literature, and guidelines to guide plans.

Skills

Clinical leadership
Regulatory insights
Data interpretation

Education

MD/DO/MBBS/MBChB
Licensed to prescribe independently

Job description

Scorpion Therapeutics in the United States seeks a Medical Director to provide Clinical Development leadership for the PF 4404 program, overseeing design, conduct, and analysis of trials while coordinating with regulatory affairs, pharmacovigilance, biostatistics, and medical affairs.

You will support clinical operations, investigators, and external stakeholders to uphold scientific, ethical, and regulatory standards.

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