Category

Description

Skills And Requirements
Understanding and experience of reporting and working with adverse events in Oncology (AESI, imAEs, risk tolerance in Oncology trials)
Utilising biomarkers, previous awareness
Ability to analyse adverse events profile and results
ISS / ISE exposure
Completed 2-3 submissions
Willingness to ask questions
Ability to pry into questionable data and challenge the figures rather than accepting, i.e, chase data leads
Interested in patient and science, not just the programming
Ensure proactive engagement with a multitude of people across study team
Previous Stakeholder management
Project management skills (especially in Lead / Principle role)
Must be competent in the disease state, experience with solid tumours (rather than haematology)
Must have worked with RECIST and understand the criteria, ask leading questions about the specifics of RECIST

Seniority Level
Mid-Senior level

Industry
Biotechnology Pharmaceuticals Medical Devices
Employment Type
Full-time

Job Functions
Engineering Information Technology

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