Clinical Research Associate
Do you enjoy research, development, and design? Do you want to build your skillset while working on a team of senior staff clinical researchers? My client, one of the world's largest medical device companies, is looking to hire a Clinical Research Associate. This position is in Santa Clara, CA.
As a Clinical Research Associate you will be responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions.
Additional responsibilities include:
- Writing basic study protocols
- Monitoring or overseeing monitoring of investigational sites to ensure protocol adherence
- Assuring timely enrollment of patients and retrieval of CRFs from study sites,
- Processing CRFs including data cleanup and classification of data, and completion of study summary
The ideal candidate will possess 5+ years of experience.
Overall, this is a wonderful opportunity to work on a team and learn from clinical researchers with a thriving company. You will have wide-range of responsibilities and the ability to grow your skillset.
If you are interested in learning more about the Clinical Research Associate opportunity, please forward me your resume and/or contact me on the details below!
Sthree US is acting as an Employment Business in relation to this vacancy.