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ProPharma

Pharmacovigilance Coordinator, Benefit Risk

ProPharma

. Support day-to-day pharmacovigilance and benefit-risk activities across assigned projects .

Posted 9/15/2026full-timeRemote • SerbiaJuniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates foundational knowledge of Pharmacovigilance and supports day-to-day activities, ensuring compliance with quality standards and client requirements. Proficient in administrative tasks, including document control, meeting coordination, and training support within the pharmacovigilance domain.

Highest-signal resume keywords
Pharmacovigilance SupportDocument ControlMeeting CoordinationMicrosoft Office ProficiencyHealthcare Knowledge

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
PharmacovigilanceDocument ControlData EntryLiterature ScreeningAudit Preparation
Soft Skills
Organizational SkillsCommunication SkillsTeam Collaboration
Tools & Technologies
Microsoft WordMicrosoft ExcelMicrosoft PowerPointWeb-Based ApplicationsElectronic Systems
Industry Keywords
PharmacyNursingLife SciencesClinical ResearchDrug Safety

About the role

Key responsibilities & impact
  • Support day-to-day pharmacovigilance and benefit-risk activities across assigned projects
  • Enter and maintain project-related information within internal systems
  • Assist with local literature screening and associated operational activities
  • Support training of affiliate personnel on relevant pharmacovigilance responsibilities
  • Coordinate meetings, prepare agendas, and distribute meeting documentation
  • Record and maintain pharmacovigilance meeting minutes and action logs
  • Manage filing, archiving, and document control activities
  • Provide administrative support to the Pharmacovigilance department and project teams
  • Assist with preparation and coordination during audits and inspections
  • Ensure activities comply with company procedures, quality standards, and client requirements
  • Contribute to continuous improvement initiatives and other duties as required

Requirements

What you’ll need
  • Bachelor's or Master's degree in Pharmacy, Nursing, Life Sciences, or another health-related discipline
  • Basic knowledge or foundational understanding of Pharmacovigilance
  • Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint
  • Experience using databases, web-based applications, or electronic systems
  • 0–1 years of experience in pharmacovigilance, healthcare, life sciences, clinical research, or a related field
  • Recent graduates with relevant academic backgrounds and an interest in drug safety are encouraged to apply

Benefits

Comp & perks
  • Remote opportunity
  • Hybrid working encouraged for new hires within a reasonably short commute of an office, as agreed with the manager
  • Career development in a global leader in regulatory and pharmacovigilance services
  • Exposure to international pharmaceutical and biotechnology clients
  • Collaboration with experienced drug safety and benefit-risk professionals
  • Development of expertise in pharmacovigilance, regulatory compliance, and safety operations
  • Opportunity to contribute to projects supporting patient safety and public health worldwide
  • Equal Opportunity Employer committed to diversity, equity, and inclusion
  • Applications personally reviewed by a member of the recruitment team
  • Applicants receive an outcome on their application