- IQVIA (Los Angeles, CA)
- …sites. + Act as the point of contact with thought leaders for investigator -initiated study (IST's) ideas within company pipeline assets. + Participate in ... assess their ability to participate in observational registries, to conduct investigator -initiated trials, participating in company sponsored studies. +… more
- Parexel (Sacramento, CA)
- …the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance ... The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (eg… more
- Gilead Sciences, Inc. (Foster City, CA)
- …including but not limited to assessment of eligibility criteria, addressing investigator questions, safety monitoring, and ensuring high data quality through data ... scientific and clinical leadership or oversight in the preparation of investigator brochures + Provide scientific and clinical leadership to cross-functional teams… more
- Gilead Sciences, Inc. (Foster City, CA)
- …are not limited to, study protocol preparation, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical ... clinical development component(s) in the preparation/review of regulatory documents, investigator brochures and development plans. + Coordinates the collection and… more
- BeOne Medicines (Emeryville, CA)
- …of safety data at safety governance meetings (Safety Management Team and Company Safety Committee) and for Safety Monitoring Committee (SMC), Data Monitoring ... development, update, and review of safety communication documents (eg, Dear Investigator Letter, Informed Consent Form, Investigator 's Brochure, Healthcare… more
- Cedars-Sinai (Los Angeles, CA)
- …timely manner. Projects may include but are not limited to investigator -initiated protocol development including protocol writing, case report form development, ... applicable. + Acts as a liaison with Principal Investigators, pharmaceutical company representatives and other project funding organizations to monitor and update… more
- J&J Family of Companies (Irvine, CA)
- …Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, ... for operating company . + Oversees/executes feasibility, selection, set up, conduct and...study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports,etc.). + Supports applicable trial registration… more
- J&J Family of Companies (Irvine, CA)
- …Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, ... for Operating Company under supervision. + Participates in the feasibility, selection,...study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports). + Supports applicable trial registration… more
- Merck (Sacramento, CA)
- …marketing, to ensure high-quality, safe, and effective products, contributing to the company mission of improving and saving lives around the world. Our Research ... Division QA Clinical Quality (CQ) provide independent assurance that our Company ensures the safety, rights, and well-being of participants, while complying… more
- Sumitomo Pharma (San Francisco, CA)
- Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient ... the collection and exchange of scientific/technical information important to the Company 's market and development portfolio. Assist in the management of… more