Director, Clinical Science

Scorpion Therapeutics; United States; Remote; USD 180,000 - 260,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Clinical Science professional to lead and execute clinical development plans for cell therapy assets, notably TIL therapies, across phases 1–4.

You will collaborate across global teams, guide data review, protocol design, and regulatory submissions, and represent Clinical Science in cross-functional programs with investigators, KOLs, and vendors; remote with travel ~25%.

Qualifications

• 7+ years oncology clinical trial experience.
• 5+ years in clinical science/clinical development.
• Advanced degree (PhD, PharmD, MD) preferred.
• Experience with cell therapy, data review, and clinical documentation.
• Strong understanding of GCP, FDA, ICH, and other regulatory standards.
• Excellent project management, communication, and analytical skills.

Responsibilities

• Contribute to global clinical development strategies.
• Support data analysis, clinical documentation, protocol design, and regulatory submissions.
• Represent Clinical Science in cross-functional teams, including collaborations with investigators, KOLs, and vendors.
• Assist in training, study site support, and communications strategies.

Skills

Oncology clinical trials

Clinical Science

Regulatory knowledge (GCP, FDA, ICH)

Data analysis

Cross-functional collaboration

Project management

Scientific communication

Education

PhD

MD

PharmD

Job description

Role

Senior Clinical Science professional supporting the development and execution of clinical development plans for cell therapy assets, specifically TIL therapy for cancer.

Responsibilities

• contribute to global clinical development strategies
• support data analysis, clinical documentation, protocol design, and regulatory submissions
• represent Clinical Science in cross-functional teams, including collaborations with investigators, KOLs, and vendors
• assist in training, study site support, and communications strategies

Requirements

• 7+ years oncology clinical trial experience
• 5+ years in clinical science/clinical development
• advanced degree (PhD, PharmD, MD) preferred
• experience with cell therapy, data review, and clinical documentation
• strong understanding of GCP, FDA, ICH, and other regulatory standards
• excellent project management, communication, and analytical skills

HighValue

focus on cell and gene therapy, tumor infiltrating lymphocytes, cancer indications, phases 1-4 development, regulatory interactions, and global clinical plans.

WorkSetup

remote with travel (~25%).