Senior Pharmacovigilance Associate

This is a fully remote position, open to applicants in Czechia.

📋 Description

• Conducting tasks within the ICSR management unit according to the established scope and timeline: Processing Individual Case Safety Reports (ICSRs)

• Executing ICSR follow-up for SAE/SUSAR Management

• Performing reconciliation (clinical, partners)

• Ensuring personal data protection

• Managing Product Quality Complaints and coordinating with Quality Assurance

• Engaging with Medical Information

• Applying MedDRA and WHO coding

• Generating Database Outputs and Reports (including data for monthly client reporting)

• Overseeing workflow and resource management

⛳️ Requirements

• Graduate in life sciences, pharmacy, nursing, or other healthcare-related fields, or equivalent experience in pharmacovigilance

• At least 1 year of professional experience in pharmacovigilance

• Strong organizational skills with a focus on detail and the ability to multitask

• Proficient management skills, including time and issue handling

• Advanced proficiency in English (both spoken and written)

• High level of proficiency in MS Office

🏝️ Benefits

• Opportunities for training and career advancement within the organization

• A strong focus on both personal and professional development

• A friendly and supportive work environment

• The chance to collaborate with colleagues from around the globe, with English as the primary language of communication