Clinical Research Associate (CRA / SCRA) - sponsor dedicated
... protocol, consent documents for ethics IRB approval, as well as preparing ...
... protocol, consent documents for ethics IRB approval, as well as preparing ...
... proper application documents to EC IRB and, where appropriate to Regulatory ...
... terms of competent authority and IRB EC REB submissions, as needed. ...
... protocol, consent documents for ethics IRB approval, as well as preparing ...
... proper application documents to EC IRB and, where appropriate to Regulatory ...
... of application documents to EC IRB at start up and for ...
... and questionnaire collection, ICF negotiations, IRB EC submissions, IMP Release and ...