
Senior Pharmacovigilance Officer, Team Lead – Case Processing Manager, Medical Device Experience
Posted Aug 6

Posted Aug 6
This is a fully remote position, open to applicants in Serbia.
• Lead a team focused on ICSR management for specific projects or groups of projects.
• Directly manage the ICSR staff.
• Assign tasks for designated projects and teams while overseeing workflow processes.
• Promote effective collaboration with clients in ICSR Management.
• Contribute to the achievement of company goals and objectives.
• Provide support for project team activities on behalf of both clients and the company.
• Develop and maintain project-specific KPIs for contracted ICSR activities.
• Enhance procedures, training, and other initiatives to boost ICSR team efficiency.
• Suggest process modifications to the ICSR Operational Lead.
• Manage ICSR deviations with guidance from the ICSR Operational Lead.
• Review trackers and timesheet data to ensure precision.
• Engage in ICSR processing and provide secondary quality control for cases.
• Assist other departments as authorized and directed by the ICSR Operational Lead.
• Serve as the subject matter expert for the assigned team.
• Provide support to the RA & PV Network Department as necessary.
• Function as the LCPPV for the specified country and PRLS for the designated language, as agreed with the line manager.
• Degree in life sciences, pharmacy, nursing, or another healthcare-related qualification, or relevant experience in pharmacovigilance.
• Significant prior experience in pharmacovigilance.
• At least 1 year of experience in a line management position.
• Experience in the medical device sector is required.
• Exceptional written and verbal communication abilities.
• Strong organizational skills, including attention to detail and the ability to multitask.
• Proficient delegation skills.
• Effective planning and time management capabilities.
• Technical proficiency.
• Ability to work collaboratively within a team.
• Fluent in English, both spoken and written.
• Advanced skills in MS Office.
• Opportunity for remote work.
• Flexible working environment.
• Opportunities for professional growth.
• Collaborative team atmosphere.
• Supportive culture emphasizing kindness, flexibility, growth, and a sense of belonging.
• Chance to collaborate with global teams across Europe, North America, South America, Asia, and Australia.
• Work alongside experts in clinical research, pharmacovigilance, and quality consulting.
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