Senior Clinical Development Director – Oncology (Hybrid)

Scorpion Therapeutics; Pennsylvania; Hybrid; USD 210,000 - 320,000; Full time

Benefits offered by this job

Relocation support

401(k) plan

Paid time off

Medical/dental/vision

Job summary

Scorpion Therapeutics in Pennsylvania seeks a Clinical Development Medical Director to lead the prifetrastat program, conducting medical monitoring, data review, and safety oversight across studies.

You will collaborate with investigators, Clinical Scientists, and regulatory authorities to shape development strategies, prepare regulatory submissions, and communicate key findings while supporting hybrid work and potential relocation.

Qualifications

• Primary medical degree from a recognized school.
• 4+ years biopharmaceutical clinical research & development experience.
• Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation.

Responsibilities

• Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring.
• Lead peer-to-peer interactions with investigators.
• Serve as point of contact for clinical issues among study teams, investigators, ethics committees, steering committees, and regulatory authorities.
• Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional teams.
• Provide clinical development leadership across several study teams.
• Represent Clinical Development on subteams including for Marketing Authorization Applications.
• Collaborate with Global Development to create/refine development strategies.
• Represent the company in external engagements/joint collaborations.
• Collaborate with Clinical Scientists to review/interpret clinical data, identify key findings, and communicate to stakeholders.
• Stay current with literature and guidelines to advise and drive current/future clinical development plans.

Education

MD/DO/MBBS/MBChB

Job description

Scorpion Therapeutics in Pennsylvania seeks a Clinical Development Medical Director to lead the prifetrastat program, conducting medical monitoring, data review, and safety oversight across studies.

You will collaborate with investigators, Clinical Scientists, and regulatory authorities to shape development strategies, prepare regulatory submissions, and communicate key findings while supporting hybrid work and potential relocation.