Clinical Data Analyst - ERP (R&D, Clinical Supply Chain)
- Ware, Hertfordshire (GBR)
- £22 - £25.9 Per Hour
- 12 Months
- Start date: ASAP
- Ref: GSK0JP00086516
- data management
- ich
- sops
- pharmaceutical
- gxp
- database development
- fda
- protocols
- manufacturing
- research
- documentation
- troubleshooting
- compliance
- templates
Clinical Data Analyst - ERP (R&D, Clinical Supply Chain)
GSK Ware/Initially Remote
12 Month Initial Contract
Pay: up to £25.90 per hour (PAYE ONLY)
Purpose
To be accountable for the data entry and data management for master data for pharmaceutical materials as part of the new Clinical Supply Chain ERP platform. This person should have a high attention to detail, strong computer skills with the ability to multi-task with minimal error. The primary responsibilities include creating, checking and approving material codes, data discrepancy management, data review and data troubleshooting. The position will perform duties in compliance with protocols, data standards and SOPs.
Critical knowledge
• Good knowledge of data management
• Good knowledge of GMP regulations and guidelines
• Knowledge of Master Data Management in a Pharmaceutical environment is preferred.
Accountabilities
Enters and manages information into a computer system to create master data into the Clinical Supply Chain ERP platform.
• Creation, checking and reviewing of master material codes and data
• Participate in the development of internal documentation and infrastructure such as SOPs and data management documents and templates to support the data management activities
• Interact with Supply Chain team members, scientists, etc to address data queries and resolve data issues
• Curate and own enterprise reference data lists for the ERP platform
• Develop deep knowledge for MDM including data, people, processes and technologies in use.
• Proactively address data quality issues before problems arise.
Critical capabilities
• Flexible, adapts work style to meet organisational needs. Ability to work proactively and effectively in a fast-paced environment.
• Ability to work collaboratively within a team
• Effective communicator, both oral and written
• Demonstrated ability to communicate with non-data focussed people
• Excellent organisational skills and ability to prioritise tasks
• Excellent computer skills and proficient use of MS Office tools
Critical experience
• Experience in data management in a pharmaceutical or other research / manufacturing setting.
• Experience in management of GxP data and associated documentation needed to meet regulatory and company standards
• Working knowledge of GMP, ICH, FDA and EMA regulations and guidelines
• Exposure to hands on database development a plus
