Operation Specialist1
IQVIA · Liaoning, China
OtherFull-timeCompany career page
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Role summary
IQVIA seeks an Operations Specialist to process and manage safety data and pharmacovigilance information across clinical research projects. The role involves data entry, adverse event tracking, quality assurance, and coordination with cross-functional teams while maintaining regulatory compliance.
What they're looking for
- Bachelor's degree in life sciences or related field
- Up to 3 years relevant experience, including up to 1 year pharmacovigilance experience
- Medical terminology knowledge and intermediate Microsoft Office proficiency
- Strong attention to detail, organizational skills, and written communication abilities
- Knowledge of safety databases and global clinical research regulatory requirements
- Ability to multitask, meet strict deadlines, and work independently or as team member
What you'll be doing
- Process and assess safety data according to regulations, SOPs, and project requirements
- Perform pharmacovigilance activities including adverse event collection, tracking, coding, and database entry
- Conduct quality reviews and identify problems, escalating issues to senior team members
- Liaise with project management, clinical, data management, and healthcare professional stakeholders
- Mentor junior team members and participate in project meetings and department initiatives
Privacy & handoff
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