This is a non-technical role that requires a person who is interested in analyzing and checking medical data records for patient safety purposes and has strong planning skills for coordinating monthly reports and reconciliation.
The candidate will be required to review pharmaceutical safety information and other pharmacovigilance data to check for accuracy and version control of these data sources.
An organized and accurate person with a high attention to detail is required for this role. Computer entry literacy is required, with confidence in the use of Microsoft Office, such as Word, Excel, and Outlook.
Daily activities include communication with colleagues, pharmaceutical companies, and other business partners, so excellent written and spoken English is required.
The successful candidate will be responsible for supporting the technical team with managing the schedules for monthly reports for clients and for communicating with external partners to carry out reconciliation activities to collect or exchange safety information.
The candidate will conduct the first phase screening and triaging of adverse event case reports received and downloaded from regulatory authorities to determine case validity using a specific set of criteria.
These elements are controlled by local and global regulations, and the candidate will need to be able to follow the processes and instructions described in company standard operating procedures and working instructions.
The candidate will be trained and closely supported during the first year as they learn about the regulatory requirements and familiarize themselves with the data elements in pharmacovigilance. Continued Professional Development is required as part of this role.
Please note that the company reserves the right to close the advert early if we receive a high volume of suitable applicants.
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