Clinical Research - Palo Alto, CA

+ Clinical Research Associate · The Clinical Research Associate (CRA) will be responsible for managing multiple aspects of clinical trials. This includes assisting with study start-up, ongoing monitoring, data management, and analysis, · Job summary: Manage multiple aspects of c ...

· Job Description · Clinical Research Coordinator · Hourly pay: $40/hr · Worksite: Leading university (Palo Alto, CA Onsite) · W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL · 40 hours/week, 5 Month Assignment, Possible extension/conversion ...

The Clinical Research Coordinator will serve as the primary contact with research participants, sponsors and regulatory agencies. This role involves coordinating studies from startup through close-out ensuring compliance with protocols and managing various aspects of clinical res ...

· Job Description · Clinical Research Coordinator · Hourly pay: $35/hr · Worksite: Leading university (Palo Alto, CA Onsite) · W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL · 40 hours/week, 5-6 Month Assignment, Possible extension/conversio ...

The Clinical Research Coordinator role involves coordinating clinical research projects including determining eligibility of study participants, collecting data for clinical research projects. · ...

A leading university seeks a Clinical Research Coordinator to join the clinical trials office. · Serve as primary contact with research participants sponsors and regulatory agencies Coordinate studies from start-up through close-out Determine eligibility of and gather consent fro ...

Clinical Research Associate to perform duties related to the coordination of clinical studies. · Serve as primary contact with research participants, sponsors, and regulatory agencies. · Determine eligibility of and gather consent from study participants according to protocol. · ...

The Clinical Trials Office in Maxonic seeks a Clinical Research Associate to perform duties related to the coordination of clinical studies. · Serve as primary contact with research participants, sponsors, and regulatory agencies. · Coordinate studies from start-up through close- ...

Clinical research coordinator for oncology studies in Palo Alto CA. Coordinates studies from start-up through close-out and serves as primary contact with research participants sponsors and regulatory agencies. · ...

Clinical research coordinator coordinates clinical trials across the full study lifecycle from start-up through close-out. · ...

Fortvita is seeking a dynamic and experienced Clinical Research Associate I or II (CRA) to manage and monitor clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practices (GCP). · ...

The Clinical Trials Office in the company seeks a Clinical Research Associate to perform duties related to the coordination of clinical studies. · ...

+Job summary · We are seeking a dedicated Clinical Research Coordinator to serve as the primary contact with research participants, sponsors and regulatory agencies. · Responsibilities:Determine eligibility of study participants and gather consent according to protocol. · Assist ...

Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. · ...

+Join our team as a Clinical Research Coordinator. · + · ++Serve as the primary contact with research participants, sponsors and regulatory agencies. · ...

School of Medicine, Stanford, California, United StatesNewResearch9 hours ago Post Date108271 Requisition # · The Division of Gastroenterology and Hepatology has a long tradition of major contributions in basic research, a new commitment to clinical and outcomes research, a ...

The Clinical Trials Office seeks a Clinical Research Associate to perform duties related to the coordination of clinical studies.The incumbent will work with the team to ensure the safety and well-being of trial participants and to document related data per protocols and SCI-CTO ...

The Clinical Research Coordinator will serve as the primary contact with research participants, sponsors, · sponsors and regulatory agencies. This role involves coordinating studies from startup through close-out, · ensuring compliance with protocols, ...

Clinical Research Coordinator I supporting the Emergency Medicine team with clinical research studies. · ...

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