Job Overview

Review, assess and process Safety data and information, across global service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team member.

Essential Functions

• Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project global requirements.

• To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events (AE)/endpoint information.

• Coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.

• Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.

• Assure 100% compliance towards all people practices and processes.

Qualifications

• An Individual with a minimum of a bachelor’s degree in scientific or healthcare discipline or allied life sciences graduation with 1-1.5 years of relevant experience required.

• English: Advanced.

• Willingness and aptitude to learn new skills across Safety service lines.

• Ensure quality of deliverables according to the agreed terms.

• Good working knowledge of Microsoft Office and web-based applications.

• Demonstration of IQVIA core values while doing daily tasks.

• Excellent attention to detail and accuracy.

• Strong organizational skills and time management skills.

• Ability to work as a Team Player, contribute and work towards achieving Team goals.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com