Global Principal Clinical Scientist: Strategy & Trials Lead

CSL; King of Prussia (PA); Hybrid; USD 140,000 - 190,000; Full time

Job summary

CSL is seeking a Senior Clinical Development Scientist to provide scientific input to clinical development strategies across multiple therapeutic areas. The role requires partnering with teams to design trial-related documents and oversee execution of programs.

You will lead development of Clinical Development Programs, author study documents, contribute to manuscripts and regulatory submissions, and mentor project teams while ensuring quality and compliance.

Qualifications

• Bachelor's degree or equivalent in Science, Allied Health or Engineering.
• 8+ years experience in the biotechnology or pharmaceutical industry (or biomedical research organization).
• 5+ years managing projects.
• In-depth knowledge in drug development and manufacturing processes for pharmaceuticals (CMC, non-clinical, clinical, Regulatory Affairs).

Responsibilities

• Provide scientific input to clinical development strategies and therapeutic areas.
• Contribute to the scientific strategy and trial document design, and oversight of trials.
• Lead development of Clinical Development Program.
• Author clinical study documents and assist with submission materials.
• Collaborate across functions to define and deliver clinical strategy.

Skills

Project management

Scientific/clinical input

Cross-functional collaboration

Education

Bachelor's degree or equivalent in Science, Allied Health or Engineering

Job description

CSL is seeking a Senior Clinical Development Scientist to provide scientific input to clinical development strategies across multiple therapeutic areas. The role requires partnering with teams to design trial-related documents and oversee execution of programs.

You will lead development of Clinical Development Programs, author study documents, contribute to manuscripts and regulatory submissions, and mentor project teams while ensuring quality and compliance.