Drug Safety Specialist

As a Safety Specialist II at PPD Philippines, you will play a crucial role in day-to-day adverse event reporting and Pharmacovigilance (PV) activities. Operating within a highly regulated environment, your responsibilities will encompass a range of activities, including but not limited to:

• Collection, monitoring, assessment, evaluation, research, and tracking of safety information
• Coordination and performance of adverse event data entry, coding, and assessment
• Case review, follow-up, tracking of reports, and regulatory reporting activities
• Effective collaboration with project team members, client contacts, investigators, adverse event reporters, and third-party vendors

Requirements:

• Proven experience in Pharmacovigilance activities
• Strong understanding of adverse event reporting processes
• Proficiency in adverse event data entry, coding, and assessment
• Ability to effectively collaborate with various stakeholders
• Excellent organizational and time-management skills
• Adherence to strict timelines and regulatory standards

Location: Fully Remote

Application Deadline: Open until the position is filled

Join PPD Philippines and be part of a dynamic team contributing to the advancement of drug safety and regulatory compliance. We embrace diversity and encourage individuals of all backgrounds to apply. Your expertise can make a significant impact in the world of drug safety!