Vacancy Description
Summary of Responsibilities
- To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax, etc.
- Receive information, record and report Adverse Drug Reaction in timelines (according to the regulations and to internal WI/SOPs) that may be received over the telephone call, email, fax, etc.
- Execute drug safety data management processes – a combination of call intake, call dialogue documentation, peer review, case follow-up, report preparation and submission to regulatory authorities.
- Perform any other support activities as assigned – tracking various types of information and metrics, ongoing QC of defined process steps, training, reconciliation of data from multiple sources.
- Team Management, Employee Management, Coaching, ensure team compliance on company policies.
- Primary resource of process or case information and guidance of team members...
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