CPRD IR Study Support Officer
The Medicines And Healthcare Products Regulatory Agency
| Location: | Canary Wharf, London |
|---|---|
| Salary: | £36,395 |
| Hours: | Full Time |
| Contract Type: | Permanent |
| Placed On: | 3rd January 2025 |
|---|---|
| Closes: | 15th January 2025 |
| Job Ref: | 383796 |
The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it aims to deliver world class regulation and improved outcomes for UK patients.
We are currently looking for an IR Study Support Officer to join our Clinical Practice Research Datalink team in the Safety and Surveillance group.
Within a week of working here, your day could look like this: supporting the development of IR platforms inlcuding the delivery and roll out of IR services via CPRD online platforms.
The successful candidate will have have a healthcare, life sciences or technical degree or equivalent work experience in a technical support role. Have previous experience in an Acceptance Testing environment.
- Be proficient in operability of online EDC systems designed to meet user requirements
- Have previous experience of supporting technical development, ideally in a clinical research environment
- Have excellent verbal and written communication skills including the ability to communicate in a clear, succinct and engaging manner.
Closing date: 15th January 2025
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