Negotiable
Undetermined
Undetermined
Slough, England, United Kingdom
Summary: A global pharmaceutical company is seeking a contractor for a Senior Process Quality Excellence Specialist role on an initial 12-month contract. The position involves working on global studies within Quality Management, focusing on SOP writing and process development. The candidate will work independently and cross-functionally to create and revise SOPs and lead process improvement initiatives. A background in Data Management and Clinical Research is essential for this role.
Key Responsibilities:
- 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 for SOPs and lead process improvement initiatives as required.
Key Skills:
- Extensive SOP writing experience.
- Data Management/Clinical Research background.
- Understanding of Data Management, Risk Management, and Data Standards processes at a clinical study level.
- Willingness to work in Slough 2 days per week.
Salary (Rate): undetermined
City: Slough
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
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