Pharmacovigilance Associate - Hybrid Rotational Program (Start ASAP)

Uc Bcf; Taguig; Hybrid; PHP 300,000 - 420,000; Full time

Job summary

A global pharmaceutical company is seeking a Pharmacovigilance Associate to monitor drug safety data and support pharma R&D. In this hybrid role, you'll assess compliance with regulatory standards and collaborate with teams to enhance processes. Ideal candidates will have 0-1 years of experience and knowledge in safety data analysis. Strong communication and attention to detail are essential. Apply soon as the role may close before the stated date.

Qualifications

• 0 - 1 years of experience in Pharma Research & Development.
• Proficiency in Pharma Research & Development focusing on safety data analysis.
• Knowledge of PV Case Processing and regulatory requirements.

Responsibilities

• Monitor and assess drug safety data for compliance.
• Collaborate with teams to enhance pharmacovigilance processes.
• Analyze adverse event reports for risk management.

Skills

Pharma Research & Development

Safety data analysis

Communication skills

Attention to detail

Adaptability

Job description

A global pharmaceutical company is seeking a Pharmacovigilance Associate to monitor drug safety data and support pharma R&D. In this hybrid role, you'll assess compliance with regulatory standards and collaborate with teams to enhance processes. Ideal candidates will have 0-1 years of experience and knowledge in safety data analysis. Strong communication and attention to detail are essential. Apply soon as the role may close before the stated date.