Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements
Job Summary
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
Be part of an innovative and forward-thinking company that collaborates to make a healthier world.
Matching Summary
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Skills & Requirements
Must-have
site monitoring visits
GCP and ICH guidelines
subject recruitment plan
protocol and study training
study site practices evaluation
Trial Master File (TMF)
Investigator's Site File (ISF)
Nice-to-have
scientific or healthcare degree
problem-solving judgment decision-making
establish effective working relationships
project management abilities development
Key Requirements
Bachelor's Degree
Excellent command of English
Basic knowledge of clinical research regulatory requirements
Good therapeutic and protocol knowledge
Proficiency in Microsoft Word, Excel and PowerPoint