Senior Director, Clinical Science – Oncology Biotech

SystImmune, Inc.; Princeton (NJ); On-site; USD 180,000 - 230,000; Full time

Benefits offered by this job

Premium medical/dental/vision

STD/LTD

401(k) match

PTO 15 days + 11 holidays

Job summary

SystImmune, Inc. in Princeton, NJ is seeking a Senior Clinical Data Lead to drive program strategy for assigned trials and contribute to regulatory submissions across hematology programs.

The role emphasizes data review, safety monitoring, and collaboration with medical experts to support registration and commercialization. The ideal candidate has a life sciences degree with 8+ years in industry, strong knowledge of ICH/GCP, and proven ability to communicate complex data clearly to

Qualifications

• Bachelor’s degree in life sciences plus an advanced degree (MS/PhD/MD).
• 8+ years in industry including pre-clinical and clinical research.
• Hematology experience preferred.
• Strong knowledge of ICH and GCP regulatory guidelines.
• Excellent written communication and data interpretation skills.

Responsibilities

• Contributes to developing the program strategy for assigned trials/compounds.
• Author regulatory documents and submission dossiers to support registration and commercialization.
• Develop eCRFs and guidelines for data collection and monitoring.
• Lead medical data review plans and summarize efficacy and safety data.
• Interact with KOLs and assist site/faceted country selection discussions.
• Coordinate committee meetings and prepare presentations for leadership.

Skills

Program strategy

Clinical data review

Regulatory submissions

Medical monitoring

Scientific communication

Cross-functional collaboration

Education

Advanced degree in life sciences

Job description

SystImmune, Inc. in Princeton, NJ is seeking a Senior Clinical Data Lead to drive program strategy for assigned trials and contribute to regulatory submissions across hematology programs.

The role emphasizes data review, safety monitoring, and collaboration with medical experts to support registration and commercialization. The ideal candidate has a life sciences degree with 8+ years in industry, strong knowledge of ICH/GCP, and proven ability to communicate complex data clearly to