About this role

Coordinate the design, planning and execution of early phase clinical trials
Oversee trials within and/or across program(s)/therapeutic areas
Conduct real-time oversight of ongoing trials to identify and mitigate issues
Co-author clinical sections of protocols, clinical investigator brochures, and regulatory documents
Manage trial and program projects including team activities

Bachelor’s degree and ≥6 years related experience, OR Master’s degree and ≥4 years related experience, OR PhD or doctorate with ≥2 years related experience
Understanding of clinical research development process from program planning to regulatory submission
Able to quickly develop a working scientific knowledge of different therapeutic areas
Ability to manage complex operations and projects under accelerated timelines
Scientific, medical and/or safety writing and reporting (at least one is required)
Knowledge of GCP, ICH guidelines and regulatory requirements

Senior Scientist, Clinical Research

Key skills