Roles & Responsibilities
• Manage day-to-day administrative activities for non-linguistic pharmacovigilance projects
• Coordinate file transfers, internal quality checks, and client deliveries
• Track project progress and ensure adherence to timelines and deadlines
• Support PV production teams to deliver high-quality outputs
• Implement and maintain Good Pharmacovigilance Practices (GVP)
• Ensure compliance with Good Documentation Practice (GDP)
• Provide project support activities as assigned by the supervisor or manager
Qualification
• Bachelor’s degree (Life Sciences, Pharmacy, or related field preferred)
Experience
• Fresh graduates or candidates with relevant exposure to pharmacovigilance, literature monitoring, or PV operations
• Strong interest in pharmacovigilance and drug safety domain
Skills
• Excellent written and spoken English communication skills
• Proficiency in MS Word, Excel, and Outlook
• Strong attention to detail and documentation accuracy
• Ability to learn and adapt to PV systems and technology platforms
• Good problem-solving and critical-thinking abilities
• Strong organizational and multitasking skills
• Ability to work independently and in a team-oriented environment
About the Organisation
TransPerfect is a global leader in language, content, and life sciences solutions, supporting pharmaceutical and biotech companies worldwide. Its Pharmacovigilance Solutions team delivers high-quality, compliant safety services, offering professionals a structured work environment, global exposure, and long-term career growth in the drug safety and pharmacovigilance domain.
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