Description
As a candidates with extensive experience in Medical Information and Safety you will be involved in the following activities:- Provide a comprehensive first line technical and scientific information service to external customers in line with company and industry standards
- Prepare and maintain all reference documents relating to safety of assigned company products
- Provide Patient Safety expertise to internal cross-functional colleagues as required
- Partake in project work as directed by Medical Information and Patient Safety Lead
- Responsible for the management of Product Quality complaints in line with local and global procedures and systems (GCM)
- Where MSLM support is not brand aligned, provide technical input into concept development of local brand promotional materials e.g. value propositions
- Contribute to the development and execution of medical brand plan
- Check and approve new local promotional material for technical accuracy
- Responsible for the production of data on file documents for internal customers for brands not supported by MSLs
- Contribute to Medical mentoring support to Development Team
- Focused Foundation Training support
- Focused FF meetings support (Launch conferences)
- Identification of areas for improvement in product knowledge in Account Teams
- Responsible for understanding and working to all relevant procedural documents, legislation and applicable codes and maintaining an accurate and up to date personal training record
- Take part in audits and inspections as required
- Receive details of spontaneous adverse events via telephone, letter or e-mail
- Report details to the central case processing group within defined time frames
- Ensure appropriate levels of follow-up with reporters to fulfil all legal and regulatory requirements
- Ensure all appropriate reports are distributed to regulatory authorities, Ethics Committees and investigators within regulated time frames
- Provide safety surveillance support to any Products of Local Opportunity (POLOs)
- Provide pharmacovigilance expertise to RMP cross-functional teams with input to formulation, implementation, maintenance and tracking of local PRMPs
Essential Educational requirements:
- Life science degree or appropriate professional qualifications
- Post graduate qualification in pharmacovigilance - desired, not essential.
This team is a strong Medical Information and patient safety team and you will gain extensive experience on various Therapeutic Area's as well as working under the guidance of an experienced, diverse manager.
If you are interested, please contact me before or on the 17th of June to submit your application.