Employer requires a Masters degree in Pharmaceutical Sciences, Biomedical Sciences, Project Management, or related field plus 6 months of experience in Pharmaceutical Sciences, Biomedical Sciences, Project Management, or related field. Experience must include 1 Trial Master File Management, 2 Data Analysis, 3 Vendor Management, 4 Review protocols, scope of work documents, project charter, and interface with the internal and externalbr teams on study progress and completion, 5 Authoring detailed study protocols for the study participants to comply with and meet all data requirements, and 6 Being point of escalation for assigned clinical study related issues.
Categories: eb3
0 Comments