Global Principal Cardiorenal Clinical Scientist

CSL; Glattbrugg; On-site; CHF 180,000 - 260,000; Full time

Job summary

CSL Behring is seeking an experienced clinical development professional to provide scientific input across therapeutic areas and to define and lead the Clinical Development Program strategy. The role involves authoring and reviewing submission documents, manuscripts, and conference abstracts, and coordinating with project teams to deliver robust development plans.

The position requires 8+ years in biotech/pharma with 5+ years of project management, and onsite work in Glattbrugg, Switzerland

Qualifications

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

Responsibilities

• Provide scientific input to clinical development strategies and therapeutic areas.
• Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full compliance of outputs.
• Contribute to the development of the scientific strategy of the clinical development plan, the design of trial related documents and the scientific oversight of clinical trials.
• Facilitate a team to define and deliver the clinical strategy within programs.
• Define scientific strategy for multiple program components.
• Lead the development of Clinical Development Program.
• Author clinical study documents and assist with development/critical review of submission documents.
• Contribute to authorship and review of manuscripts and conference abstracts.
• Collaboratively develop the clinical development strategy with project teams, providing input, guidance and mentorship for project teams.
• Contribute to the scientific analysis and interpretation of clinical data and the writing of clinical study reports, internal and external scientific meeting presentations and peer-reviewed publications, and all regulatory submission documents.
• Foster close collaboration with other departments, defining and improving interfaces to other departments.

Skills

Project management

Drug development knowledge

Education

Bachelor's degree in Science, Allied Health or Engineering

Job description

CSL Behring is seeking an experienced clinical development professional to provide scientific input across therapeutic areas and to define and lead the Clinical Development Program strategy. The role involves authoring and reviewing submission documents, manuscripts, and conference abstracts, and coordinating with project teams to deliver robust development plans.

The position requires 8+ years in biotech/pharma with 5+ years of project management, and onsite work in Glattbrugg, Switzerland