Director, Clinical Science - Oncology

Scorpion Therapeutics

United States

Remote

USD 180,000 - 275,000

Full time

14 days+
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Job summary

Scorpion Therapeutics seeks a Director of Clinical Science - Oncology to lead design, oversight, and interpretation of radiopharmaceutical clinical studies across oncology indications. The role demands strategic leadership, cross-functional collaboration, and clear scientific communication for publications, presentations, and regulatory submissions while advancing programs from IND to registration.

You will collaborate with investigators and external experts, ensure adherence to GxP and ICH

Qualifications

  • Advanced degree in a relevant field and strong leadership experience in oncology or radiopharmaceuticals.
  • Experience leading clinical development programs across phases I-III.
  • Proven ability to author study documents and interact with regulatory bodies.

Responsibilities

  • Design, oversight, and interpretation of radiopharmaceutical oncology studies.
  • Oversee study execution with cross-functional teams and ensure data quality.
  • Support regulatory submissions and facilitate scientific communications (publications/presentations).
  • Collaborate with investigators, external experts, and stakeholders to advance programs from IND to registration.

Skills

Leadership
Cross-functional leadership
Clinical development
Scientific communication
Regulatory submissions

Education

MD/PhD/PharmD

Job description

Role: Director, Clinical Science - Oncology

leading design, oversight, and interpretation of clinical studies for radiopharmaceuticals across oncology indications.


Responsibilities

develop clinical protocols, author key study documents (e.g., CRFs, reports), oversee study execution with cross-functional teams, ensure data quality, support regulatory submissions, and facilitate scientific communication including publications and presentations.


Collaborates with investigators, external experts, and stakeholders to advance clinical programs from IND to registration.


Requirements

advanced degree (MD, PhD, PharmD), 7-10 years in pharma, with oncology or radiopharmaceutical experience preferred; deep knowledge of GxP, ICH, and clinical development across phases I-III; proven leadership in complex, matrixed environments, with excellent communication skills.


High Value

oncology/radiopharmaceutical focus, clinical development (Phases I-III), regulatory interactions, study protocol development, GxP adherence.


Work Setup

remote within the US, with approximately 25% overnight travel.

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