Adverse Event Intake Specialist with English language
2 tygodni temu
- Performing Pharmacovigilance activities per project requirement.
- Collecting and tracking incoming Adverse Events and endpoint information.
- Receiving, reviewing and interpreting medical reports.
- Processing safety data according to applicable regulations, guidelines, Standard Operating Procedures (SOPs) and project requirements.
- Determining initial/update status of incoming events.
- Coding Adverse Events and Products, writing narratives, and performing Literature related activities as per internal/project timelines.
- Ensure to meet quality, productivity, and delivery standards per project requirements.
- Identify quality problems, if any, and bring them to the attention of senior team members.
- Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
- Bachelor's Degree in Life Science or healthcare related discipline is required.
- Excellent written and verbal skills in English (min. C1).
- Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.
- Excellent attention to detail and accuracy maintaining consistently high-quality standards.
- Excellent organizational skills and time management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
- Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.
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Adverse Event Intake Specialist with English language
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Adverse Event Intake Specialist with English language
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