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As a Clinical Research Associate I, you will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study.
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Act as the primary liaison between Principal Investigator, Senior Management, study team, sponsor, regulatory agencies/committees, UCLA Investigational Drug Services (IDS) Pharmacy, and appropriate departments (Laboratory, Radiology, Pathology, Cardiology, CTRC, etc.
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Throughout its history, the Criminal Investigator has accomplished this mission through a tradition of honor, integrity and a commitment to excellence. Please Note: The Secret Service prohibits employees from having visible body markings (including but not limited to tattoos, body art, and branding) on the head, face, neck, hand and fingers (any area below the wrist bone) (exception: a single conservative and unobtrusive tattoo in the form of a ring is authorized on one finger.
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The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Must have experience with Principal Investigator initiated studies, including study setup, source documentation, etc. Software Guidance & Assistance, Inc., (SGA), is searching for an Clinical Research Coordinator for a Contract assignment with one of our premier Healthcare clients in Los Angeles, CA.
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As an INVESTIGATOR (SPECIAL AGENT) you will be responsible for the following duties: -Assist with conducting Federal Personnel Background Investigations, many of which are sensitive or controversial, where allegations, hearsay information, or other vague or intangible information of an adverse nature exist.
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In this role, you will be responsible for preparation, submission and maintenance of regulatory applications to fulfill research requirements for open studies in addition to working with Sponsor monitors to timely process, review and collect regulatory documents maintained in the Investigator Site File. All work should be completed according to good clinical practice (GCP), JCCC CRU standard operating policies (SOP), UCLA Institutional Review Board (IRB) and government regulations.
$24.28 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Serves as sub-Investigator for clinical research studies conducted by a supervising principal investigator. Collaborate closely with study investigator informing on relevant adverse events and serious adverse events according to procedures outlined in the protocol.
$70 an hourPart-timeExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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Description The Principal Investigator is seeking an experienced, motivated, and attentive to detail research assistant with interest in neurology education research. In addition to data management, other duties of this position include reviewing scientific and medical education literature, and editing/proofreading manuscripts and grants.
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The budget specialist is responsible for reviewing the Medicare coverage analysis, protocol, sponsor proposed budget and informed consent (if available) and fully accounting for all clinical costs and investigator and study team effort required to carry out the study, as well as costs for ancillary services.
$81,873.83 - $95,000.04 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Demonstrates competence in writing, editing, and reviewing clinical study reports, investigator brochures, registration dossier modules, and other clinical regulatory documents per company and other guidelines.
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Serve as a primary benefits investigator, problem solver, and analyzer (ACA tracking, benefits auditing/billing, benefits tracking,). Manage benefits-related billing issues; investigate and run Workday custom reports to ensure that correct benefit groups are correct on the health and welfare benefits (medical, dental, vision, life insurance, AD&D, supplemental insurance monthly; MetLife voluntary benefits bi-weekly and semi-monthly; WageWorks/COBRA monthly; Bank of America/HSA bi-weekly and semi-monthly, EAP, and Group Legal.
$72,500 - $103,314 a yearFull-timeExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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You’ll build a strong rapport with your clients and have the support of a paralegal, legal assistant and legal investigator for each case that you represent. A national plaintiff’s law firm with a focus on public advocacy has partnered with Staffing Technologies in their search for a committed Litigation Associate to support their growing clientele.
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Inform and provide a detailed written explanation of the termination/suspension of the trial to the IRB and, if the investigator terminates the trial without prior agreement, to the study sponsor.
$225,000 - $275,000 a yearFull-timeExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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The ideal candidate will have a strong command of data management and survey administration, with a particular interest in candidates with experience using and creating Qualtrics surveys. This new team is being developed to better develop and study novel innovations in neurology education, such as targeted curriculum development, simulation, case-based teaching, flipped classroom learning, etc.
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investigator job in Los Angeles, CA
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