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Equivalent Experience
Description:
- Ensure clinical study data are accurate via source verification, query initiation and resolution
- Ensure sites are following the clinical study protocol, GCP, and all applicable regulations
- Conduct study site selection, qualification, training, start up, and close out
- Support IRB submissions
- Act as a primary contact between the site and the study sponsor
- Ensure proper inventory, storage, shipment, and tracking of study materials
- Ensure proper handling, storage, tracking, and shipment of clinical specimens
- Assist with data entry as necessary
- Maintain Trial Master Files for all assigned clinical studies
About Actalent:
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.