Posted: Mar 1, 2026
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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