Clinical Research Associate
Avispa TechnologyPalo Alto, CA, US5 days ago
Job type
- Full-time
Job descriptionAssemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact. Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements Participate in monitoring visits and regulatory audits. 1-2 years of experience in clinical research, with a preference for expertise in oncology, pediatric oncology, and early-phase studies. Bachelor's degree in a related medical field. Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. Ability to quickly assimilate new information and adapt to changing environments. Knowledge of medical terminology. Proficiency with Microsoft Office, Outlook, Box, etc. Proven ability to make meaningful contributions from the very beginning. 9 am-5 pm with some flexibility.
Job Description
Clinical Research Associate 1422918
- Hourly pay : $35 / hr
- Worksite : Leading university (Palo Alto, CA 94304 - Hybrid, May require occasional local and overnight travel)
- W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
- 32 hours / week, 2 Month Assignment, Possible extension / conversion
A leading university is seeking a Clinical Research Associate The successful candidate will primarily collect / manage patient and laboratory data for clinical research projects, manage research project databases, develop flowcharts and other study-related documents, and complete study documents and case report forms. The company offers a great work environment!
Clinical Research Associate Responsibilities :
Clinical Research Associate Qualifications :
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Clinical Research Associate • Palo Alto, CA, US