The study director has overall responsibility for the technical conduct of the study, as well as for the interpretation, analysis, documentation and reporting of results and represents the single point of study control. Serves as the study director for routine/compendial biocompatibility studies (primarily GLP). Schedules tests/studies. Evaluates, analyzes, and interprets data and presents in a clear, well organized, scientifically sound report. Has direct sponsor contact.
Education
Requires a Bachelor of Science in a scientific discipline.
Experience
2-3 years previous study director, laboratory or quality assurance experience required. Project management experience strongly preferred.
Requirements
Demonstrated knowledge of a laboratory, basic analysis of scientific data, basic technical writing, organizational and communication skills. Ability to effectively interact with sponsors/client representatives.
For more information or to apply for this position, please contact hr@namsa.com.
