Clinical Research Coordinator Jobs in San Francisco, CA

Job Title: Part-Time Clinical Research Coordinator Hours: Onsite 18 per week Schedule: 3 days / 6 hours each (Monday-Friday) Contract duration: Open-ended contract Job Description Join our dynamic team as a Clinical Data Coordinator specializing in an Infectious disease study. This part-time position offers a 18-hour work week where you will play a vital role in advancing clinical research. This role required you to be within a commutable distance from San Francisco, CA and will not provide rel…

Description This is a new clinical research coordinator posting. UCSF is one of the sites in this multicenter prospective study called “THRIVE”. The purpose of this research study is comparing the patient experiences of two common types of anesthesia (total intravenous anesthesia with propofol versus a volatile anesthetic). The study is collecting electronic health record data and gathering data using wearable devices and smartphone applications. In conjunction with the primary investigator, th…

Description This is a limited appointment. We are looking for a Clinical Research Coordinator who is passionate about addressing health disparities, as well having a familiarity with chronic disease management and clinical trials. This position will function as a member of a multidisciplinary research team and as someone who has experience working in care settings serving low-income patients. Experience working with racially, ethnically diverse, and lower health literacy patient populations is …

Description This is a six (6) month limited appointment. The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating a…

About Nudge At Nudge, our mission is to develop the best technology for interfacing with the brain to improve people's lives. We're starting with an approach that we believe can help the most people the fastest, and also allow us to learn as much about the brain as possible: developing a non-invasive, ultrasound-based device that can stimulate and image the brain at high resolution and depth. This is a vertically integrated effort building cutting-edge hardware, software, and research capabilit…

Organization: CPMC-California Pacific Med Center Position Overview: Collects, compiles and presents clinical data for assigned area, ensuring accuracy, timeliness and accessibility of information. Maintains clinical and/or research databases for identified programs/ specialty clinics. Collects data used for multiple purposes, which may include process improvement activities and clinical effectiveness/research studies. May prepare information for patient/family education and/ or participate in c…

San Francisco, CA · On-site · Full-time Compensation: $170,000–$250,000 0.5%–1.5% equity About the Company A seed-stage company building AI agents that automate patient recruitment for clinical trials, coordinating across SMS, voice, and email to help research sites cut the costly delays that hold trials back — a $600B market where delays cost $600K–$8M per day. The platform is already deployed at scale, battle-tested across 500K patient interactions, 190 sites, and 300 trials, and is backed b…

Description This is a targeted posting for a Clinical Research Coordinator with experience in psychedelic research to support an NIA-funded, multisite clinical trials consortium. This role is critical to advancing the study. The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI); will coordinate the data collec…

Position Definition : This position will serve as a program manager and senior clinical research coordinator for a large research program who is capable of making difficult decisions independently. As a program manager, this person will be directly responsible for overseeing a diverse portfolio of research activities for multiple studies and overseeing a research team. The portfolio may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical …

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the 1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFR CT Analysis—provides a color-coded, 3D model of a patient’s coronary arteries indicating the impact blockages have on blood flow to the heart. Heartflow is the first AI-driven non-invasive integ…

OVERVIEW: The Staff Research Associate II independently coordinates and is accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge and skills. They may provide leadership to lower-level clinical research coordinators and/or other support personnel. The primary purpose of the SRAII is to provide independent coordination for industry and PI initiated studies focusing on prostate cancer research. The position is responsible for, and …

Organization: CPMC-California Pacific Med Center Pacific Position Overview: Manages and provides operational leadership to all clinical trials staff, and overall clinical trials programs and operations, which may include one or more teams performing related work. Plans, organizes, and directs 24/7 operations and resources to ensure effective and efficient delivery of services and/or achievement of business results. Establishes protocols and practices, ensuring compliance with department, affili…

Job Description The Medical Affairs organization provides patients, healthcare providers, and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively, throughout the product lifecycle and the patient’s journey. The Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline provides medical and scientific input into core strategic and operational pipeline medical affairs activiti…

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Linke…

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Linke…