Not specified; details provided later in hiring pr...
Fully remote
Formal medical qualifications md or equivalent
Clinical drug development experience
Pharmacovigilance and gxp knowledge
The role involves developing and maintaining an expert understanding of the safety profile of assigned products while contributing to strategic safety assessments
Job Summary
The role involves developing and maintaining an expert understanding of the safety profile of assigned products while contributing to strategic safety assessments.
Candidates will be responsible for individual and aggregate case reporting activities including ICSR management and aggregate reporting such as DSUR and PBRER.
Roche offers a culture that encourages personal expression and genuine connections where every voice matters in the mission to prevent, stop, and cure diseases.
Matching Summary
The role involves developing and maintaining an expert understanding of the safety profile of assigned products while contributing to strategic safety assessments.
Salary
Not specified; details provided later in hiring process based on location
Skills & Requirements
Must-have
Formal medical qualifications MD or equivalent
Clinical drug development experience
Pharmacovigilance and GxP knowledge
Signal detection and case reporting expertise
Regulatory submission preparation skills
Nice-to-have
Board certification in relevant medical specialty
Fluency in Mandarin and English languages
Experience with remote global team collaboration
Strong presentation and communication skills
Ability to mentor junior scientists
Key Requirements
MD, MB BS, or MB ChB degree required
Minimum 4 years clinical drug development experience
At least 2 years in clinical drug safety role
Post-graduate experience in relevant clinical specialties