Pharmacovigilance Associate

Celltrion Inc; Philippines; On-site; PHP 300,000 - 520,000; Full time

Job summary

Celltrion Inc in the Philippines is seeking a Pharmacovigilance Associate to support drug safety operations through the review, processing, and assessment of adverse event reports, ensuring timely case handling and high data integrity.

The role involves drafting concise case narratives, performing initial assessments, maintaining trackers and quality records, and ensuring compliance with SOPs and global pharmacovigilance standards.

Qualifications

• Bachelor’s degree in Pharmacy, Nursing, Life Sciences, or related discipline.
• Fresh graduates or candidates with at least 1 year of relevant experience.
• Experience in pharmacovigilance, healthcare, clinical, retail pharmacy, or research is an advantage.
• Strong English communication skills, both written and verbal.
• Excellent attention to detail, organization, and time management skills.
• Proficiency in MS Office and familiarity with databases/safety systems is a plus.

Responsibilities

• Review and process adverse event and product safety reports within required timelines.
• Perform accurate case data entry, coding, and duplicate checks in safety databases.
• Draft concise and medically accurate case narratives and follow-up queries.
• Conduct initial case assessments based on established procedures and guidelines.
• Maintain documentation, trackers, and quality records related to case processing.
• Ensure compliance with internal SOPs, quality standards, and regulatory requirements.
• Collaborate with internal stakeholders to support workflow continuity and team objectives.
• Participate in training, process improvement, and cross-functional initiatives.

Skills

Strong English communication

Attention to detail

Time management

Independent worker

Multicultural teamwork

Education

Bachelor’s degree in Pharmacy, Nursing, Life Sciences

Tools

MS Office

Safety databases

Job description

The Pharmacovigilance Associate is responsible for supporting drug safety operations through the review, processing, and assessment of adverse event reports. This role ensures accurate data handling, timely case processing, and compliance with global pharmacovigilance standards while contributing to patient safety and regulatory obligations.

Key Responsibilities

• Review and process adverse event and product safety reports within required timelines
• Perform accurate case data entry, coding, and duplicate checks in safety databases
• Draft concise and medically accurate case narratives and follow-up queries
• Conduct initial case assessments based on established procedures and guidelines
• Maintain documentation, trackers, and quality records related to case processing
• Ensure compliance with internal SOPs, quality standards, and regulatory requirements
• Collaborate with internal stakeholders to support workflow continuity and team objectives
• Participate in training, process improvement, and cross-functional initiatives

Requirements

• Bachelor’s degree in Pharmacy, Nursing, Life Sciences, or related healthcare discipline
• Fresh graduates who are former CGSDCI interns, or candidates with at least 1 year of relevant experience, are welcome to apply
• Experience in pharmacovigilance, healthcare, clinical, retail pharmacy, or research is an advantage
• Strong English communication skills, both written and verbal
• Excellent attention to detail, organization, and time management skills
• Ability to work independently and in a fast-paced environment
• Proficiency in MS Office and familiarity with databases/safety systems is a plus
• Strong teamwork skills with the ability to work in multicultural environments