Senior Clinical Scientist
Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown.
We are seeking an experienced Senior Clinical Scientist to join our growing Clinical Development team, to drive early-phase development in oncology and endocrinology indications. Reporting to VP of Clinical Development and in collaboration with a Medical Director, you will integrate preclinical findings into clinical strategies and design Phase 1-2 clinical trials, author clinical study protocols and regulatory filings (INDs and CTAs) to advance novel drug candidates into clinic, execute early phase studies, and deliver proof-of-concept.
How you might spend your days
- Study design and strategy: evaluating preclinical data and scientific concepts to develop clinical study Protocols, Investigator’s Brochures (IBs), Informed Consent Forms (ICFs) for Phase 1–2 dose escalation and expansion studies
- Regulatory submissions: authoring clinical sections for global IND and CTA submissions, responding to inquiries from health authorities (FDA, EMA, HC), preparing protocol amendments, and contributing to Clinical Study Reports (CSRs)
- Medical monitoring and patient safety oversight
