- Cedars-Sinai (Los Angeles, CA)
- …makes effective contributions to the section, and adheres to the Cedars-Sinai compliance plan, code of conduct, and hospital and departmental policies and ... and transforming data to the necessary formats. + Provides solutions for investigator 's problems through data mining and extraction. + Identifies, evaluates, and… more
- AbbVie (Irvine, CA)
- …. Job Description *Must be willing to come onsite in Irvine, CA 3 days/week Oversees the direction, planning, execution, and interpretation of clinical trials or ... Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and… more
- Cedars-Sinai (Los Angeles, CA)
- …and/or clinical activities, including but not limited to, budgetary/financial compliance , preparation of grant proposals, and creating independent presentations. Not ... etc.). + Organizes clinical/research trials in conjunction with the Principal Investigator and sponsor and/or funding source. + Monitors and ensures … more
- Merck (South San Francisco, CA)
- …definitive/Good Laboratory Practice (GLP)], serving as a contributing scientist/principal investigator on toxicity studies, and executing PK/TK strategies to support ... a high standard in accordance with external and internal regulations. + Ensure compliance with GLP, SOPs, and study protocols. + Deliver high quality scientific… more
- IQVIA (Carlsbad, CA)
- …a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront ... Quality Assurance: Assess site practices for protocol adherence and regulatory compliance , escalating quality issues as needed. Study Progress Management: Oversee… more
- Cedars-Sinai (Los Angeles, CA)
- …and/or clinical activities, including but not limited to, budgetary/financial compliance , preparation of grant proposals, and creating independent presentations. Not ... etc.). + Organizes clinical/research trials in conjunction with the Principal Investigator and sponsor and/or funding source. + Monitors and ensures … more
- Medtronic (Los Angeles, CA)
- …of didactic sessions, case studies and other training-related presentations at investigator and research coordinator meetings and other training events. + Educate ... or relevant hospital experience)_ **Nice to Have (Preferred Qualifications):** + 3 + years Structural Heart industry field experience (TAVR, Mitral, Tricuspid, LAAC,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and reviews routine regulatory documents to ensure that CROs are in compliance with protocols, regulatory requirements, SOPs, and monitoring plans. + May be ... required to present at internal or external meetings (ie, investigator meetings). + Leads or otherwise assists in the...**Minimum Education & Experience** + MA / MS with 3 + years' relevant clinical or related experience in life… more
- ICON Clinical Research (Los Angeles, CA)
- …trials. + Other Interfaces: Study Responsible Physician, Regional Quality and Compliance . Manager/Specialist, Local Drug Safety Officer (where required) and Site ... a major airport + Have a minimum of 2 - 3 years' experience in monitoring pharmaceutical industry clinical trials...at assigned sites + Ability to partner closely with investigator and site staff to meet all of our… more
- Providence (Anaheim, CA)
- …research studies. This role is responsible for interfacing with the Principal Investigator , Patient, Sponsor, and the IRB. This position is directly responsible to ... and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not...+ 2 years experience in a Clinical Research setting. 3 years preferred. **Why Join Providence?** Our best-in-class benefits… more