Senior Clinical Scientist, Hematology Clinical Development

CSL Vifor; Waltham (MA); Hybrid; USD 168,000 - 199,000; Full time

Job summary

CSL Vifor is seeking a highly experienced scientist to contribute to hematology clinical development programs, from strategy through regulatory submissions.

You will collaborate with internal and external stakeholders to ensure high-quality outputs, oversee safety and data integrity, and potentially lead the Clinical Development Program. A strong background in R&D and CRO oversight is essential.

Qualifications

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

Responsibilities

• Contribute to scientific development of clinical programs and studies in hematology
• Provide scientific and clinical input for safe, efficient execution of programs
• Author or contribute to documents aligned with scientific strategy (CDP, protocols, ICF, manuals)
• Develop medical monitoring oversight strategy to ensure patient safety and data integrity
• Lead development of Clinical Development Program when needed
• Contribute to authorship of manuscripts and abstracts
• Collaborate with stakeholders to translate strategy into deliverables
• Assist in writing regulatory submissions and study reports
• Manage liaisons for external study oversight committees

Skills

Cross-functional collaboration

Communication

Attention to detail

Independent work

Problem-solving

CRO oversight

Education

PhD

Master's degree

Bachelor's degree in Science

PMP Certification

Job description

CSL Vifor is seeking a highly experienced scientist to contribute to hematology clinical development programs, from strategy through regulatory submissions.

You will collaborate with internal and external stakeholders to ensure high-quality outputs, oversee safety and data integrity, and potentially lead the Clinical Development Program. A strong background in R&D and CRO oversight is essential.