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Are you a life science graduate? Or are you a healthcare professional with similar experience?
Client Details
My client is a outsourcing provider of medical information enquiry handling and pharmacovigilance services to various clients within the pharmaceutical industry.
HQ based in Milton Keynes
Description
Drug Safety Associate
The successful candidate will be responsible for participating in the collection, safety review, processing and reporting of adverse event data in compliance with applicable local and global regulations and company standard operating procedures.
They will perform accurate computer data entry of identified adverse event information, ensure timely processing and where necessary report these to regulatory authorities. The Drug Safety Administrator will be an active participant in meetings and assist the PV Manager in maintaining standard operating procedures or working practices. During their daily activities, the Drug Safety Administrator will be required to liaise with pharmaceutical companies and other business partners.
Profile
- Life science graduate (1-2 years working experience desirable) or other allied healthcare professional.
- Someone who can work alone, plan and prioritise his or her assignments under strict timelines.
Job Offer
- Membership to Private Healthcare Scheme on completion of probation.
- Hybrid working arrangements for full time staff.
- Access to corporate discounts.
- Membership to Company Pension Scheme.
