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

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

📋 Description

• Oversee the team dedicated to ICSR management for specific projects or groups of projects.

• Manage ICSR personnel directly.

• Allocate tasks among assigned projects and teams while supervising the workflow.

• Facilitate effective collaboration with clients in ICSR Management.

• Contribute to organizational goals and objectives under the guidance of the ICSR Operational Lead.

• Assist other project team activities on behalf of both the client and the company.

• Develop and maintain project-specific KPIs for contracted ICSR activities.

• Enhance procedures, training, and other initiatives to boost ICSR team productivity.

• Suggest process improvements to the ICSR Operational Lead.

• Manage ICSR deviations with assistance from the ICSR Operational Lead.

• Review trackers and timesheet data to ensure accuracy.

• Engage in ICSR processing and conduct second-level quality control of cases.

• Provide support to other departments as directed.

• Act as the designated team subject matter expert.

• Support the RA & PV Network Department, including serving as LCPPV for the specified country and PRLS for the designated language.

⛳️ Requirements

• Graduate in life sciences, pharmacy, nursing, or another healthcare-related field, or possess relevant experience in pharmacovigilance.

• Significant prior experience in pharmacovigilance.

• At least 1 year of experience in a supervisory role.

• Required experience with medical devices.

• Exceptional written and verbal communication skills.

• Strong organizational skills, attention to detail, and ability to multitask.

• Proficient in delegation.

• Skills in planning and time management.

• Strong technical abilities.

• Ability to work effectively in a team.

• Fluent in spoken and written English.

• Advanced proficiency in MS Office.

🏝️ Benefits

• Option for remote work.

• Collaborative team atmosphere.

• Flexible workplace culture.

• Opportunities for growth.

• Supportive work environment.

• Chance to engage in global projects.

• Opportunity to contribute to patient safety.

• Collaborate with experts in clinical research, pharmacovigilance, and quality consulting.