Safety Reporting Administrator-150041
We have a new opening for a Safety Reporting Administrator to join our Cambridge based Pharmacovigilance (PVG) team.
Reporting to a Safety Administration Manager, the Safety Reporting Administrator has responsibility for the tracking of all documents related to the department's designated projects. Working within the department, the SA will process all documents and information on time, to appropriate quality standards and within the allocated time constraints. The SA will also assist the project team and PVG Team Manager by producing study metrics as required.
For projects assigned to your team, you will ensure that day to day tracking (data entry) and filing of Serious Adverse Events, follow-up information and all study documents occur in line with standard systems and Standard Operating Procedures/Working Practice Documents within the appropriate time frame. You will also assist with the development of any tracking databases prior to production, the production of appropriate SOPs/WPD's or guidelines, and with the filing/archiving of project documents as needed.
The successful candidates will have:
• Good organisational skills
• Excellent attention to detail particularly when entering data
• Good keyboard skills
• Ability to work to strict deadlines
• Good English language and grammar skills
• Good oral and written communication skills
• Good knowledge of MS Office (including MS Word and Excel)
A can do attitude is essential, as well as the ability to prioritise and multi-task. You must be able to work as part of a wider team but must be able to work on your own initiative also. You must also thrive in a fast paced environment and easily adapt to changing processes.