Regulatory Information Rim Specialist/analyst
1 month ago
Regulatory Information Specialist - Remote (UK), 6 Month Contract
Working with a well-established Global CRO who work with the top pharmaceutical companies in the UK. You will be working with the US and the UK Regulatory Information team.
**Your new role**
This is a 6 month initial Regulatory Information Specialist contract where you will be responsible for executing and overseeing the entry and verification of data into the RIM Systems and databases. You will have enough Regulatory Information experience thatyou can mentor the junior members to ensure the data is compliant and up to standard. You will be the Subject Matter experience with Veeva RIM within the team and maintain expert knowledge of regulations, legislations.
To be successful you will have:
- Extensive experience working with Veeva RIM / Liquent Insights for registrations
- Life Sciences background
- Organised and analytical thinker
- Experience supporting migration/ tech transfer projects related to RIM (desired)
This is a 6-month contract with scope for extension. It is fully remote but you must be located and have right to work in the UK.
**What you need to do now**
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
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