The Safety Associate, IQVIA Safety Operations team, will review, assess and process safety data and information, across service lines, received from various sources and distribute reports onwards to both internal and external third parties, following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. 

Key responsibilities: 

Performing Pharmacovigilance activities per project requirement.

Collecting and tracking incoming Adverse Events and endpoint information.

Receiving, reviewing and interpretation of 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 a senior team members.  

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

Minimum Required Education and Experience 

Bachelor’s Degree in Life Science or healthcare related discipline is required

Excellent written and verbal skills in English (min. C1)