marked devices Responsible for writing Clinical Investigation Plans Provide clinical input into product development Knowledge of research methodology – clinical investigation design and biostatistics included Experience
marked devices Responsible for writing Clinical Investigation Plans Provide clinical input into product development Knowledge of research methodology – clinical investigation design and biostatistics included Experience
method validation, instrument qualification. OOS investigation and documentation experience. Author Environmental
method validation, instrument qualification. OOS investigation and documentation experience. Author Environmental
study progress to project leaders and principal investigators Maintain study site documentation following
study progress to project leaders and principal investigators Maintain study site documentation following
study progress to project leaders and principal investigators
daily and weekly statistics to the principal investigator and senior study personnel as and when required
daily and weekly statistics to the principal investigator and senior study personnel as and when required
daily and weekly statistics to the principal investigator and senior study personnel as and when requ