You will co-ordinate all communications with the technical team, Quality Assurance and the Sponsor. Independently programs in SAS to generate tables, listings and graphs for clinical study reports and submissions of data to global regulatory agencies. Experience with gas and vapour detection, environmental testing.
Report to the manager.
These staff provide the high level product knowledge and skills to present The company Informatics products to potential and existing customers.
Determine specific needs of end users; design and implement software, etc. Degree in Chemistry or related discipline. In this role you will be responsible for study design, protocol preparation, in-life study conduct and monitoring, data evaluation and interpretation and reporting. Surgical skills and experience of animal experimentation in large animals will be desirable. Police the protocols within manufacturing. Design and develop examples for demonstrations. Designing and running experiments. You will co-ordinate all communications with the technical team, Quality Assurance and the Sponsor.
In this role you will be responsible for study design, protocol preparation, in-life study conduct and monitoring, data evaluation and interpretation and reporting.
Develop medical SOPs. Determine specific needs of end users; design and implement software, etc. Designing and running experiments.
Work with Business Analysts, gather functional requirements, and ensure that supported data model conforms to these requirements as well as modeling standards.
Plan and document testing tasks. Define and implement data warehouse transformations; develop and manage ETL processes for warehouse and data mart build and maintenance.
Apply innovative techniques in designing and unit testing of the product. BW agent detection and analysis of data. Validation of the processes related to new and existing products.