Senior Clinical Development Scientist

Scorpion Therapeutics; Parsippany-Troy Hills (NJ); On-site; USD 180,000 - 280,000; Full time

Job summary

Scorpion Therapeutics in New Jersey is seeking a senior clinical development scientist to support late-stage oncology programs. You will collaborate with the Clinical Scientist Program Lead on trial activities including protocol design, study execution and data analysis.

Responsibilities include developing study concepts, preparing protocols and regulatory documents, contributing to data reviews and scientific presentations, and assisting with study coordination and regulatory compliance,

Qualifications

• PharmD or PhD in clinical research/pharmacology with 6+ years' experience, or MS with 8+ years in scientific/drug development.
• Knowledge of clinical trial design, GxP, FDA/EMA regulations, and biopharma industry standards.

Responsibilities

• Develop study concepts.
• Prepare protocols and regulatory documents.
• Contribute to data review and scientific presentations.
• Assist with study coordination and regulatory compliance.
• Primarily within cancer therapies such as CAR T-cell treatments.

Skills

Clinical trial design

GxP compliance

FDA/EMA regulations

Cross-functional collaboration

Education

PharmD or PhD in clinical research/pharmacology

MS in scientific/drug development

Job description

Role: Support late-stage oncology clinical development, collaborating with the Clinical Scientist Program Lead on trial activities including protocol design, study execution, and data analysis.

Responsibilities

• develop study concepts
• prepare protocols and regulatory documents
• contribute to data review and scientific presentations
• and assist with study coordination and regulatory compliance
• primarily within cancer therapies such as CAR T-cell treatments.

Requirements

• PharmD or PhD in clinical research/pharmacology with 6+ years' experience, or MS with 8+ years in scientific/drug development
• knowledge of clinical trial design, GxP, FDA/EMA regulations, and biopharma industry standards

Preferred

• experience in Multiple Myeloma or CAR T-cell therapies

HighValue

• oncology
• late-stage clinical trials
• regulatory submissions
• GxP compliance
• cross-functional collaboration

WorkSetup: Not specified; travel may be required.