Scientific input to clinical development strategies
Translation of development plan into operational deliverables
Scientific content of clinical program documents
CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients
Job Summary
CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients.
You will be responsible for scientific input to clinical development strategies, acting as the primary liaison between the assigned therapeutic area and key stakeholders to ensure translation of the development plan into operational deliverables.
Contribution to the scientific content of clinical program documents is a key deliverable and includes study synopses and protocols, investigator’s brochures, informed consent forms, clinical study reports, medical monitoring plans, conference abstracts, internal and external scientific meeting presentations, and peer-reviewed publications.
Matching Summary
CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients.
Skills & Requirements
Must-have
scientific input to clinical development strategies
translation of development plan into operational deliverables
scientific content of clinical program documents
scientific and clinical development input
scientific oversight of clinical trials
Nice-to-have
agile team
collaboration
patient impact
future-ready team
Key Requirements
8+ years experience in biotech/pharma
5+ years in managing projects
Bachelor's degree or equivalent in Science, Allied Health or Engineering