AE Safety Associate At IQVIA
Key responsibilities:
-To Prioritize and complete the
assigned trainings on time.
-Receiving, reviewing and
interpretation of medical report.
-Process safety data according to
applicable regulations, guidelines, Standard Operating procedures (SOPs) and
project requirements.
-To 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.
-Ensure to meet quality standards
per project requirements.
-Ensure to meet productivity and
delivery standards per project requirements.
-To ensure compliance to all
project related processes and activities.
-Creating, maintaining and
tracking cases as applicable to the project plan.
-Identify quality problems, if any,
and bring them to the attention of a senior team member.
-To demonstrate problem solving
capabilities.
Attend project team meetings and
provide feedback to operations manager on any challenges/issues or successes.
-100% compliance towards all people practices and processes
-Perform other duties as assigned.
Minimum Required Education and Experience
-Must be Fluent in English and
Arabic
-Life Science Degree
Skills and Abilities
-Excellent attention to detail and
accuracy.
-Good knowledge of medical
terminology.
-Working knowledge of applicable
Safety Database.
-Self-motivated and flexible.
-Ability to follow
instructions/guidelines, utilize initiative and work independently.