- Sharp HealthCare (San Diego, CA)
- …San Diego **Department** **Job Status** Regular **Shift** Day **FTE** 1 **Shift Start Time** **Shift End Time** Certified Case Manager (CCM) - Commission for ... Association (ACMA); Master's Degree; Bachelor's Degree in Nursing **Hours** **:** **Shift Start Time:** 8 AM **Shift End Time:** 4:30 PM **AWS Hours Requirement:**… more
- Stanford University (Stanford, CA)
- …you bring to the position. **Specific Tasks include:** + Coordinate studies from start - up through close-out. + Determine eligibility of and gather consent from ... audit study forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed. +… more
- Sharp HealthCare (San Diego, CA)
- …San Diego **Department** **Job Status** Regular **Shift** Day **FTE** 1 **Shift Start Time** **Shift End Time** Bachelor's Degree **Hours** **:** **Shift Start ... members, providers, other health plan departments, and representatives of regulatory agencies. + Customer serviceProvides prompt, accurate and excellent services… more
- Bristol Myers Squibb (San Diego, CA)
- …aspects of protocol conduct, both early and late phase, including protocol writing, start - up , study execution, analysis and reporting. + Experience in working ... development plans in GU cancers. Responsibilities include support for IND preparation, regulatory authority interactions, design and execution of Phase 1 to Phase 3… more
- IQVIA (Carlsbad, CA)
- …(CRF) completion and submission, and data query generation and resolution. May support start - up phase. * Ensure copies/originals (as required) site documents are ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
- Gilead Sciences, Inc. (Foster City, CA)
- …needed. + Ability to manage any component of full cycle study management, from start - up to close-out. + Advanced knowledge of study management best practices and ... trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports… more
- Amgen (Thousand Oaks, CA)
- …by internal and external collaborators, investigators, and consultants + Provide input/review study start up documentation, eg, CRF design + Attend and provide ... range of audiences, including executive leadership, development partners, and global regulatory agencies. This role will include global development leadership of one… more
- IQVIA (Carlsbad, CA)
- …(CRF) completion and submission, and data query generation and resolution. May support start - up phase. * Ensure copies/originals (as required) site documents are ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
- Bristol Myers Squibb (San Diego, CA)
- …and adequate endpoints + Understands clinical trial operational complexities from study start up through enrollment, quality assurance, and study readout + ... with the cross functional GPT members + Participates in regulatory filings (NDA, BLA filings) as well as develops...a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply… more
- Sharp HealthCare (San Diego, CA)
- …San Diego **Department** **Job Status** Regular **Shift** Day **FTE** 1 **Shift Start Time** **Shift End Time** California Physicians and Surgeons License - Medical ... of CA; Doctor of Medicine (MD) **Hours** **:** **Shift Start Time:** Variable **Shift End Time:** Variable **AWS Hours...community relations. + Assures plan conformance with legal and regulatory requirements + Assists the Chief Medical Officer and… more