- University of Southern California (Los Angeles, CA)
- …has an immediate opening for a Project Assistant to assist the principal investigator in the day-to-day operations of the Outreach, Recruitment and Engagement Core ... scientists, among others. Under the supervision of the principal investigator , the Project Assistant will coordinate and implement outreach, education,… more
- The County of Los Angeles (Los Angeles, CA)
- …high-risk areas and its compliance to policies and procedures; determining whether internal controls are adequate to address inherent risks within administrative and ... findings and recommendations of results. Identifies areas with deficiencies in internal controls, conflicting policies, and best practices. Plans, conducts, and… more
- Terumo Neuro (Aliso Viejo, CA)
- …working with MicroVention departments and clients to set and meet internal and external deliverables. Some typical job duties include: + Collaborating ... study reports + Briefing documents + Previous human experience summaries + Investigator brochures + Study protocols + Medical literature analysis reports +… more
- Abbott (Santa Clara, CA)
- …of abstracts, presentations, and publications of clinical study data, working with investigator authors and internal teams. + Synthesize literature and ... high employer contribution + Tuition reimbursement, the Freedom 2 Save (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU… more
- J&J Family of Companies (Irvine, CA)
- …This role is based in Irvine, CA and reports to the office on assigned days 2 -3 times per week. At Johnson & Johnson, we believe health is everything. Our strength ... (CSER) Team responsible for global evidence dissemination of scientific findings from investigator led clinical trials and registries sponsored by Johnson & Johnson… more
- Bristol Myers Squibb (San Diego, CA)
- …+ Clinical Study Protocols and Amendments + Informed Consent Forms (ICFs) + Investigator Brochures (IBs) + Clinical Study Reports (CSRs) + Clinical sections of ... all documents comply with regulatory guidelines (ICH, FDA, EMA), internal RayzeBio SOPs, and company style guides. + Interpret...the pharmaceutical, biotech, or CRO industry. + At least 2 years of experience managing medical writing projects or… more
- Medtronic (CA)
- …the assigned review committee and/or the sponsor. + Coordinate communication between internal and external customers to facilitate shipping and return of product ... of didactic sessions, case studies and other training-related presentations at investigator and research coordinator meetings and other training events. + Educate… more
- University of Southern California (San Diego, CA)
- …Agreements/specification, CRF Data Entry Manual) + Provides study updates at the Internal and Executive calls + Manages External Data Service Provider contracted to ... such as the serious adverse event + Presents at investigator 's meetings and helps lead data management training +...assigned REQUIREMENTS: + Bachelor's Degree + Minimum of two ( 2 ) years of on hands Clinical Data Management experience… more
- University of Southern California (Los Angeles, CA)
- …At times will provide information regarding time or effort to facilitate budget set up. 2 . Ensures that study is conducted as written so that scientific questions are ... dose modifications based on toxicity may be necessary and require recalculation. 2 . Protocol Compliancea. Ensures correct date for return clinic appointment or… more
- Bristol Myers Squibb (Los Angeles, CA)
- …our medical mission to be recognized as the trusted partner for internal stakeholders and the healthcare community, driving scientific exchange to enhance medical ... partner with HCPs on disease state initiatives, collaborative research projects, and investigator sponsored research (ISR) of interest and in alignment with BMS… more