Clinical Research Coordinator

Clinical Research Coordinator 1472789

• Hourly pay: $40/hr
• Worksite: Leading university (Palo Alto, CA 94304 - Onsite)
• W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
• 40 hours/week, 5 Month Assignment, Possible extension/conversion

A leading university is seeking a Clinical Research Coordinator. The successful candidate will conduct clinical research and work independently on progressively more complex projects/assignments, and independently manage significant and key aspects of a large study or all aspects of one or more small research studies. The company offers a great work environment!

Clinical Research Coordinator Responsibilities:

• Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials
• Oversee data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data.
• Formally supervise, train, and/or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work.
• Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to requests and questions.
• Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance.

Clinical Research Coordinator Qualifications:

• 2+ years of experience in clinical research.
• Bachelor's degree in a related field.
• Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
• A valid California non-commercial Class C Driver's License, if applicable.
• Proficiency in Microsoft Office and database applications.
• Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
• Knowledge of medical terminology.
• Ability to drive day or night, if applicable.
• Oncology.
• Onsite clinical coordinator (no pharma, CRO, etc.).
• Treatment Phase I trials.

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