PV Officer, Medical Devices

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

📋 Description

• Offer assistance to various activities carried out by the project team on behalf of both the client and the company.

• Establish and uphold project-specific KPIs for contracted ICSR activities.

• Enhance procedures, training sessions, and other initiatives to boost the efficiency of the ICSR team.

• Suggest process modifications to the ICSR Operational Lead.

• Oversee ICSR deviations with the support of the ICSR Operational Lead.

• Review trackers and timesheet information to ensure precision.

• Process ICSR cases and conduct a secondary quality control of those cases.

• Assist other departments as required.

• Function as the designated team subject matter expert.

• Provide support to the RA & PV Network Department as necessary.

• Serve as the LCPPV for the specified country and PRLS for the assigned language, as coordinated with the line manager.

⛳️ Requirements

• A degree in life sciences, pharmacy, nursing, or another healthcare-related qualification, or relevant experience in pharmacovigilance.

• 3–4 years of professional experience in pharmacovigilance.

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

• Required experience in medical devices.

• Outstanding written and verbal communication abilities.

• Strong organizational skills, with a focus on 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.

• Fluency in English, both spoken and written.

🏝️ Benefits

• Opportunity for remote work.

• A flexible working environment.

• Potential for growth and advancement.

• A collaborative and supportive team culture.

• Work with global teams across Europe, North America, South America, Asia, and Australia.

• Contribute to patient safety and pharmaceutical treatment.

• Join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.