As a Senior Drug Safety Associate, you will join a leading clinical research organization, dedicated to an innovative Pharma developing prescription biopharmaceutical medications. You will be responsible for processing and overseeing adverse event/drug experience reports (serious and non-serious) for marketed products and clinical trials, leading the case management lifecycle. The position is homebased in Switzerland.
Requirements
- Bachelor’s degree in a science or healthcare related discipline (nursing/pharmacy preferred), or equivalent.
- Minimum of 4 years pharmacovigilance experience or other equivalent clinical or pharmaceutical experience.
- Proficiency using safety database systems (Argus experience preferred).
- Advanced knowledge of global Pharmacovigilance regulations (CFR/GVP), ICH Guidelines and Good Clinical Practices.
- Excellent computer skills (i.e. Microsoft Word, Excel, Outlook, and Power Point).
- Excellent ability to work effectively within a team environment.
- Advanced organizational, time management, and problem-solving skills.
- Ability to create and deliver presentations.
- Excellent verbal and written communication skills.
- Fluency in written and verbal English
Benefits
- Various annual leave entitlements
- A range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
Originally posted on Himalayas
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