- Austin, TX
What you'll be doing
- Assisting with the review of data using scientific judgement regarding the quality and integrity of data and records associated with assigned studies. The project director gives the final approval. Assisting with communications with analysts and other personnel involved in conducting the studies. Assisting with conducting/ensuring the study is in accordance with applicable SOPs, GLPs, and protocols. Assisting in scheduling and coordinating to maintain the flow of assigned projects. Assisting to ensure quality of deliverables including data, reports, and electronic files. Communicating effectively internally with all levels of personnel. Assisting to write/prepare/review PIFs, Analytical test methods, reports, SOPs, protocols, and proposals. Assisting to ensure the study data and supporting records are archived in a timely manner. Performing other miscellaneous duties as assigned.
What your background should be
- GLP, QA, and QC experience strongly preferred. Highly developed organizational and time management skills. Communicates effectively with technical and upper level management. Ability to understand graphs, tables, charts, and perform calculations needed for the task, usually associated with 1-year on-the-job training. Ability to report data and procedures orally and in writing.
Required Schooling / Training
- Bachelor degree
Who is the client company
- The company concern about medicine and healthcare services.
- If you are interested in this position, send your resume to email@example.com