Position: Clinical Research Associate I
Location : Sunnyvale-CA
Duration : 6+ Months with possible extension
Description and Requirements:
Description: Assist Clinical Study Coordinator in execution of onsite Clinical Studies. Able to take direction in fast paced environment and to be self-directed, when Coordinator is not available. Needs to possess excellent interpersonal skills to consent, screen and schedule Research Subjects. Role requires highly acute attention to detail and MS proficiency (Excel, Word) to manage study operational data. Provide administrative and office support. Previous experience in research is highly desirable. Must be flexible with availability depending on business needs.
Duties include (but are not limited to):
• Assist Lead Study Coordinator as needed with:
o completing and maintaining study documentation, including study binders, paper study documents, and electronic study documents such as consent forms, screening forms, enrollment logs, and ultrasound device documentation.
o preparing IRB submissions & applications such as yearly Continuing Review Application
o completing protocol deviation reports and adverse event reporting
o providing support to Study Staff (engineers, clinical specialists)
o coordinating & conducting training activities
o coordinating and overseeing regular Monitoring visits
• Screen and Schedule Research Volunteers
• Consent Volunteers
• Escort Volunteers
• Compensate Volunteers
• Data Entry
Please send me your updated copy of resume along with the best number to reach you ASAP.
APN Software Services, Inc.
39899 Balentine Drive, Suite 385, Newark, CA 94560
Direct: 510.870.8798 | Fax: 510.623.5055 | email@example.com