28/05/2024 | Fulltime | Hillingdon | PharmiwebSuch as contributing to and reviewing user requirements for new GPS systems, contributing to computer system validation documentation, and performing support of reporting platform(s) change controls, and represent the GPS Systems team in projects. The position may be called upon to assist with training end users
Save for later28/05/2024 | Fulltime | Sheffield | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later28/05/2024 | Fulltime | Derby | PharmiwebRegulatory requirements - Responsible for the overall design, scientific and technical conduct of studies, including interpretation, analysis, documentation and reporting of results - Initiate and maintain continuous client communication throughout the development and conduct of studies and to ensure Client
Save for later28/05/2024 | Fulltime | Merthyr Tydfil | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later28/05/2024 | Fulltime | Hillingdon | PharmiwebSupports feasibility assessment to select relevant regions and countries - Oversees and provides input to the development of study specific documentation including but not limited to case report form (CRF), data management plan, monitoring plan, monitoring oversight plan, etc. - Reviews site level
Save for later28/05/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later28/05/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later28/05/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later28/05/2024 | Fulltime | PharmiwebTo ensure that all data management operations are conducted to SOPs; contribute to the ongoing revision/improvement of these SOPs. - Creation of project specific documentation for assigned trials, i.e. the Data Management Plan and the Data Management File. - Prepare database and edit check specifications
Save for later28/05/2024 | Fulltime | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
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