AE Management Associate - 12 Month Secondment
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
Vigilance is essential to guarantee the ongoing understanding of the profile of adverse events related to the use of Reckitt’s medicinal products, medical devices, cosmetics and vitamins, minerals and supplements (VMS).
This role is a crucial role since the post-holder is responsible for completing the key tasks in the provision of safety services and vigilance to facilitate and support the ongoing marketing of RECKITT medicinal products, medical devices, cosmetics and VMS.
The safety function is a statutory function imposed by external regulators.
Your responsibilities
- AE Management - Associate is accountable overall to the AE Management - Manager, Global PV & Deputy QPPV & Director- Risk Management & Vigilance, European Union (EU) QPPV and Senior Vigilance Manager.
- AE Management - Associate is directly accountable to, on a day-to-day basis, to the AE Management – Manager.
- Specific tasks and responsibilities include, but are not limited to:
- Working with the AE Management - Manager and under the executive guidance from senior management to ensure all responsibilities regarding the processing (triage/entry/coding/evaluation/reporting/admin) of adverse event reports related to Reckitt’s medicinal products, medical devices, cosmetics and VMS is to a high standard, completed on time and according to regulations, domestic and foreign reporting requirements, general quality standards, Global Standard Operating Procedures and Reckitt values.
- Ensuring that all electronic records and paper records and the safety database are managed and maintained accordingly as per Standard Operating Procedure with specific actions taken from the AE Management – Manager.
- Ensuring that output from the group is of high quality and quality checks completed and in line with relevant industry requirements and Standard Operating Procedures.
- Ensuring AE Management team requests/queries and tasks, including ad hoc, are completed in a timely manner and according to industry requirements and Standard Operating Procedures.
- Ensuring the GVG mailbox is monitored and managed on a daily basis (business days).
- Ensure that DSO in local operating countries receive support as appropriate for the management for safety reports and database requirements.
- Work with the AE Management – Manager to ensure that the third-party case processors receive documentation as appropriate for case processing. Training and support of third-party case processors members with guidance from the Team Leader.
- Ensuring that all reports of adverse events related to Reckitt’s medicinal products, medical devices, cosmetics and VMS are processed in a timely fashion to ensure safety reports and PSURs are delivered to the appropriate regulatory authority on time and any ad hoc search requirements from the safety database can be delivered to the requester as required.
- Work with the AE Management - Manager to ensure that the SOP, working documents and other appropriate documentation are updated and current in line with standard operating procedures, industry regulations and direction from the Team Leader and senior management. Focus is allocated subject to business needs at the discretion of the manager.
The experience we're looking for
- RAS experience across product classifications with an understanding of appropriate pharmacovigilance legislation, including but not exclusively the Good Pharmacovigilance Practice (GVP)
- Good attention to detail; prove ability to quality check and analyse medical and scientific dates including medical coding using regulatory dictionaries.
- Good communication skills and confidence in representing the functiona externally (audits/inspections with regulatory bodies), and internally (not limited to RAS); maintaning Reckitt's legal obligations and embedding safety requirements and output in all that Reckitt does.
The skills for success
What we offer
Equality
Job Segment:
Medical Device, Counseling, Medical Coding, Pharmacovigilance, Nutrition, Healthcare