Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines
Job Summary
Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines.
Perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming - Adverse Events(AE)/endpoint information determining initial/update status of incoming events database entry coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Matching Summary
Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines.
Skills & Requirements
Must-have
Process Safety data
Pharmacovigilance activities
database entry
coding AE and Products
writing narratives
Literature related activities
Nice-to-have
demonstrate problem solving capabilities
flexible and receptive to changing process demands
willingness and aptitude to learn new skills
work towards achieving Team goals
Key Requirements
High School Diploma or equivalent
Bachelor's degree in life sciences or related field
up to 3 years of relevant experience
up to 1 year of Pharmacovigilance experience
Good knowledge of medical terminology
Working knowledge of applicable Safety Database
Knowledge of applicable global, regional, local clinical research regulatory requirements