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Global Project Head, Solid Tumor Antibody Drug Conjugates; ADCs

Job in Morristown, Morris County, New Jersey, 07960, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-07-08
Job specializations:
  • Pharmaceutical
    Oncology, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 150000 - 200000 USD Yearly USD 150000.00 200000.00 YEAR
Job Description & How to Apply Below
Position: Global Project Head, Solid Tumor Antibody Drug Conjugates (ADCs)

Key Responsibilities

  • Drive worldwide clinical development and life cycle management for a late-stage Solid Tumor Oncology antibody drug conjugate (ADC) compound.
  • Lead the Global Product Team (GPT) to ensure optimal global compound development strategy in collaboration with the Global Brand Team (GBT).
  • Own compound clinical development strategy and execution, including studies for regulatory purposes and budget planning.
  • Lead cross‑functional GPT planning and implementation of end‑to‑end compound strategy (translational, regulatory, drug manufacturing, safety, medical, and commercial compound leads).
  • Represent Clinical Development within the cross‑functional GBT for commercial brand strategy.
  • Present and discuss development strategy with internal stakeholders, external investigators, advisory boards, and worldwide regulatory authorities.
  • Contribute to Solid Tumor Oncology and cross‑asset Disease Area strategies; assess external business development opportunities in Hematopoietic Stem Cell Transplantation and, if applicable, lead implementation.
Requirements
  • MD or PhD.
  • 7+ years of experience in clinical development in Solid Tumor Oncology (biotech or pharmaceutical industry).
  • Thorough understanding of global drug development and functional roles/responsibilities.
  • Proven leadership of high‑performing cross‑functional clinical development teams.
  • Experience with successful marketing authorization submissions.
  • Excellent written and verbal communication skills.
  • 20% domestic and international travel.
Preferred Qualifications
  • Experience leading pivotal trials for regulatory approval in solid tumor oncology.
  • Experience preparing regulatory submissions; discussion/negotiation with health authorities.
  • Experience collaborating with commercial and medical functions in launch and/or post‑launch.
  • Experience working in a matrix environment and in regional alliance partnerships/co‑development.
  • Ability to integrate new information, adapt to evolving data/external landscape, and build internal/external networks.
Benefits
  • Health and wellbeing benefits, including high‑quality healthcare, prevention and wellness programs, and at least 14 weeks’ gender‑neutral parental leave.
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