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

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

📋 Description

• Oversee the team tasked with ICSR management for designated projects or project groups.

• Manage ICSR personnel directly.

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

• Foster effective collaboration with clients in ICSR Management.

• Contribute to the achievement of company goals and objectives.

• Provide assistance to project team activities on behalf of clients and the organization.

• 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 information to ensure precision.

• Engage in ICSR processing and perform secondary quality control of cases.

• Assist other departments as directed.

• Function as the designated team subject matter expert.

• Support the RA & PV Network Department, including serving as LCPPV for a specific country and PRLS for a particular language.

⛳️ Requirements

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

• Substantial prior experience in pharmacovigilance.

• At least 1 year of experience in a line management capacity.

• Experience with medical devices is essential.

• Exceptional written and verbal communication abilities.

• Strong organizational skills, with a focus on detail and multitasking.

• Proficient delegation skills.

• Effective planning and time management capabilities.

• Technical competencies.

• Ability to work well in a team environment.

• Proficient in English, both spoken and written.

• Advanced proficiency in MS Office applications.

🏝️ Benefits

• Opportunity to work remotely.

• Flexible working conditions.

• Opportunities for professional growth.

• Supportive and collaborative team culture.

• Chance to collaborate with global teams.

• Enthusiastic team of experts in clinical research, pharmacovigilance, and quality consulting.