Job Description
A global pharmaceutical company is looking to hire a contractor on an initial 12 month contract. Working on global studies within the Quality Management area, the successful candidate will be responsible for SOP writing and developing processes.
* Work independently and cross-functionally on SOPs and initiatives.
* Create new processes and revise existing documents.
* Provide support where needed for the SOPs and lead process improvement initiatives as required.
* The ideal candidate would have an understanding of Data Management, Risk Management, and Data Standards processes at a clinical study level
Required:
* Extensive SOP writing experience
* Data Management/Clinical Research background
* Willingness to work in Slough 2 days per week