Senior Clinical Scientist, Hematology Programs (Hybrid)

CSL Vifor; King of Prussia (PA); Hybrid; USD 168,000 - 199,000; Full time

Job summary

CSL Vifor is seeking a scientifically skilled professional to contribute to hematology clinical development programs. You will ensure high-quality outputs, lead or contribute to program documents, and collaborate across cross-functional teams to translate strategy into actionable deliverables.

The role demands deep knowledge of drug development processes, strong communication, and the ability to drive safety and data integrity across studies with CRO oversight experience.

Qualifications

• PhD, MSc or BSc in a science field; advanced degree preferred.
• 4+ years (PhD); 6+ years (MS); or 8+ years (BS) in R&D in biotech/pharma.
• 3+ years of clinical development research experience.
• Knowledge of drug development and manufacturing processes (CMC, non-clinical, clinical, regulatory).

Responsibilities

• Contributes to scientific development of clinical programs and studies in Hematology.
• Provides input for safe, efficient, timely execution of programs with high quality outputs.
• Author or contribute to program/study documents and training materials aligned with strategy.
• Develops medical monitoring oversight strategy to ensure patient safety and data integrity.
• May lead development of Clinical Development Program.
• Contributes to authorship/review of manuscripts and conference abstracts.
• Collaborates with internal/external stakeholders to translate strategy into deliverables.
• Contributes to analysis/interpretation of data and writing of reports/publications and regulatory documents.
• Manages processes and liaisons to support external study oversight committees.

Skills

Cross-functional collaboration

Excellent communication

Attention to detail

Independent & team work

Problem solving

CRO oversight experience

Education

PhD / MSc / BSc in Science

Job description

CSL Vifor is seeking a scientifically skilled professional to contribute to hematology clinical development programs. You will ensure high-quality outputs, lead or contribute to program documents, and collaborate across cross-functional teams to translate strategy into actionable deliverables.

The role demands deep knowledge of drug development processes, strong communication, and the ability to drive safety and data integrity across studies with CRO oversight experience.