- Cordis (Irvine, CA)
- …unmet and critical medical needs. **Responsibilities** The **Senior Clinical Research Associate (Coronary)** role is a key position within the coronary program ... adherence to appropriate US and OUS regulations, compliance with the study Protocol (s), and applicable local regulations + Manage and maintain internal Trial Master… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …Remote options may be considered within the US. As an ** Associate Director, Quantitative Pharmacology, Pharmacometrics,** you will support all **pharmacometrics** ... **Job Description** + Conduct **pharmacometrics** activities related to study design, protocol development, study execution, reporting and interpretation of data. +… more
- Parexel (Glendale, CA)
- **Job Posting:** Onsite Research Associate - Bilingual in English and Japanese Parexel Early Phase Clinical Unit supports the development of innovative new medicines ... information systems and computer programs. + Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of… more
- US Tech Solutions (Mountain View, CA)
- …of computational and experimental scientists. The client is seeking a Research Associate with a background in analytical chemistry for a contract position. ... including both HPLC and GC repairs and maintenance. + Assist protocol development for a metabolomic pipeline, including sample processing and extractions.… more
- Ricoh Americas Corporation (Palo Alto, CA)
- …file conversion, file naming, and encryption tasks. + Perform FTP (File Transfer Protocol ) for printing and manage Table of Contents for electronic files. + Perform ... Optical Character Recognition (OCR) tasks and file formatting for printing in Microsoft Office Suite and Adobe Acrobat Pro. + Conduct daily quality checks on convenience copiers and respond to errors or troubleshooting copy machines. + Maintain daily meter and… more
- Abbott (Alameda, CA)
- …activities and overall site management ensuring compliance to the Study Protocol , Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department ... procedures and applicable regulatory requirements. + Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization (CRO) selection and management,… more
- Abbott (Riverside, CA)
- …procedures. + Familiarity with cath lab and operating room procedures and protocol + Demonstrate advanced knowledge of cardiac pacing systems. + Must apply ... engineering skills and abilities to interpret and solve complex clinical problems + Must possess strong written and verbal communication skills, along with excellent interpersonal, presentation, analytical, and organizational abilities. Additionally, must be… more
- America's Best (San Diego, CA)
- …screens, and forwards incoming phone calls in accordance with National Vision protocol . + Diligently maintains the cleanliness of all equipment, workstations and the ... overall facility on a daily based on safety protocols. + Ensures inventory control and loss prevention procedures are followed at all times. + Maintains visual merchandising according to Brand and Company Standards. Are you the right fit? - The Suitable Talent… more
- ThermoFisher Scientific (Carlsbad, CA)
- …+ Ensure studies are conducted and documented in accordance with the study protocol , SOPs, GCP and other applicable regulatory requirements. + Collect all clinical ... study essential documents. + Participate in lab assessment visits. + Ensure that CRO activities and timelines are in coordination with project requirements. + Implement and document communication with CRO and laboratories to ensure project progress. + Timely… more
- IQVIA (Carlsbad, CA)
- …subject recruitment plan + Establishing regular lines of communication plus administering protocol and related study training to assigned sites + Evaluating the ... quality and integrity of site practices - escalating quality issues as appropriate + Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating… more