Senior Clinical Development Scientist, Hematology (Hybrid)

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

Job summary

CSL Behring is seeking a physician-scientist to contribute to hematology clinical development programs. The role focuses on scientific input for program execution, regulatory alignment, and high-quality outputs across study documents and training materials.

You will help shape medical monitoring strategies, collaborate with cross-functional teams, and support data interpretation for clinical study reports and regulatory submissions.

Qualifications

• PhD, MSc or Bachelor's in a science field.
• 3+ years of clinical development research experience.
• Strong knowledge of drug development and manufacturing (CMC, non-clinical, clinical, Regulatory Affairs).
• PMP certification preferred.

Responsibilities

• Contributes to scientific development of clinical development programs within Hematology.
• Provides input for safe, efficient execution of assigned programs ensuring quality and compliance.
• Authors/Contributes to documents (CDP, IB, protocols, eCRF, ICF, study manuals, trainings).
• Develops medical monitoring oversight strategy to ensure patient safety and data integrity.

Skills

Clinical development

Regulatory affairs

Data integrity

CRO oversight

Education

PhD

Master's

Bachelor's

Job description

CSL Behring is seeking a physician-scientist to contribute to hematology clinical development programs. The role focuses on scientific input for program execution, regulatory alignment, and high-quality outputs across study documents and training materials.

You will help shape medical monitoring strategies, collaborate with cross-functional teams, and support data interpretation for clinical study reports and regulatory submissions.