- Merck (South San Francisco, CA)
- … studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug ... into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human disease in… more
- US Tech Solutions (Mountain View, CA)
- …. **Responsibilities:** + Manage and support the setup and execution of research studies + Understand study needs, create research plans, organize study ... to conduct qualitative and quantitative research (eg, usability testing, perceptual studies , surveys, interviews). The UX Research Associate will conduct research… more
- Cedars-Sinai (Beverly Hills, CA)
- …Description** The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- Abbott (Santa Clara, CA)
- …**Work On** This position will work closely within the clinical study team including the medical director, biostatistician, project management, data management, ... and other clinical study personnel. This position will have significant interaction with...position will: + Support design of clinical trials and studies in collaboration with internal stake holders including clinical… more
- IQVIA (Carlsbad, CA)
- …located. Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study ... with project needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines of communication with… more
- AbbVie (Irvine, CA)
- …markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff. *May have ... responsibility for leading clinical study teams, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining… more
- Stanford University (Stanford, CA)
- …primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility of and ... gather consent from study participants according to protocol. Assist in developing recruitment...Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case… more
- BeOne Medicines (San Mateo, CA)
- …and amendments o Informed consent documents; + Investigator Brochures o Clinical study reports; + Abstracts, posters and manuscripts o Clinical sections of INDs ... other functional areas for the successful implementation and execution of clinical studies . + Provide scientific expertise for selection of investigator and vendors.… more
- Cedars-Sinai (Los Angeles, CA)
- …The Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, ... queries. This role is responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other… more
- IQVIA (Carlsbad, CA)
- …Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study ... with project needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines of communication with… more