Description
We are seeking a Safety Data Coordinator to review, assess and process safety data and information across service lines. The successful candidate will prioritize and complete assigned trainings on time, process safety data according to applicable regulations and guidelines, and perform pharmacovigilance activities.
Responsibilities:
- Process safety data according to applicable regulations, guidelines, and project requirements
- Perform pharmacovigilance activities, including collecting and tracking adverse events, determining initial/update status of incoming events, database entry, coding, and writing narratives
- Ensure quality standards and productivity are met per project requirements
- Liaise with different functional team members, such as project management, clinical, and data management
- Identify quality problems and bring them to the attention of senior team members
- Mentor new team members, if assigned
Requirements:
- High school diploma or equivalent in a scientific or healthcare discipline
- Bachelor's degree in life sciences or related field and up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience
- Good knowledge of medical terminology and working knowledge of safety databases and internal/client applications
- Excellent attention to detail and accuracy, with strong organizational and time management skills
- Strong verbal and written communication skills, with ability to work independently and as part of a team
Benefits:
- Competitive salary
- Opportunities for professional growth and development
- Collaborative and dynamic work environment