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Research Associate
1 week ago
InsideHigherEd Los Angeles, United States· Research Associate · University of California Los Angeles · Budgeted Pay Scale: · Full Salary Range: USD $26.48/Hr. - USD $53.40/Hr. · Department Summary · The UCLA Labor Occupational Safety and Health (LOSH) Program is dedicated to promoting worker health, safety, and wellbe ...
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Research Associate
4 days ago
Insight Global Los Angeles, United StatesMust Haves: · Bachelor's degree and/or at least one year of professional work experience · Experience with research or following work processes (gathering requirements, capturing notes, documentation). Any clinical experience can work as well. · Customer service experience. Abili ...
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Research Associate
1 week ago
University of Southern California Los Angeles, United StatesResearch AssociateApply \_REQ /apply) Keck School of Medicine Los Angeles, California · USC's Keck School of Medicine, Department of Pathology, Southern California Research Center for ALPD and Cirrhosis, is seeking a Research Associate to join its team. · We are seeking for a c ...
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Research Associate
1 week ago
New York University Los Angeles, United States Part timeSummary · : · The Institute of Human Development and Social Change (IHDSC) at New York University (NYU) is currently seeking a dedicated, detail-oriented, part-time Research Associate in to support qualitative research activities for a guaranteed-income project based in Los Ange ...
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Research Associate
1 week ago
University of Southern California Los Angeles, United StatesResearch AssociateApply \_REQ /apply) Keck School of Medicine Los Angeles, California · USC Department of Surgery recruiting a Research Associate. The Research Associate will plans, design and conduct highly technical and complex research projects independently and in consultati ...
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Research Associate
2 weeks ago
University of California - Los Angeles (UCLA) Los Angeles, United StatesThe Research Associate conducts research on worker safety & health and employment issues in California, with a particular focus on low-wage, immigrant, and/or non-English-speaking workers and those in high-risk industries. The Research Associate will plan, coordinate, and impleme ...
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Research Associate
1 week ago
Trust Co of West Los Angeles, United StatesPosition Summary · The Associate is a part of the Credit Research team within the Fixed Income Group. The Associate will work with experienced credit analysts to monitor positions and generate investment recommendations for our bank loan portfolios. The ideal candidate should hav ...
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Research Associate
1 week ago
University of Southern California Los Angeles, United StatesResearch AssociateApply \_REQ /apply) Keck School of Medicine Los Angeles, California · USC's Keck School of Medicine, Department of Medicine, is seeking a Research Associate. · The University of Southern California (USC), founded in 1880, is the largest private employer in the ...
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Research Associate
6 hours ago
University of California - Los Angeles (UCLA) Los Angeles, United StatesThe Research Associate conducts research on worker safety & health and employment issues in California, with a particular focus on low-wage, immigrant, and/or non-English-speaking workers and those in high-risk industries. The Research Associate will plan, coordinate, and impleme ...
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Research Associate
1 week ago
University of Southern California Los Angeles, United StatesResearch AssociateApply \_REQ /apply) Keck School of Medicine Los Angeles, California · A Research Associate position is available in the lab of Dr. Charleston Chiang at USC. TheChiang lab ) utilizes cutting-edge analytic tools to address questions at the intersection of human m ...
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Research Associate
1 week ago
New York University Los Angeles, United States Part timeSummary · : · The Institute of Human Development and Social Change (IHDSC) at New York University (NYU) is currently seeking a dedicated, detail-oriented, part-time Research Associate in to support qualitative research activities for a guaranteed-income project based in Los Ang ...
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Research Associate
1 week ago
University of Southern California Los Angeles, United StatesResearch AssociateApply \_REQ /apply) Keck School of Medicine Los Angeles, California · The USC Roski Eye Institute, Department of Ophthalmology, is seeking a highly trained professional to fill the position of Research Associate, located on the Health Science Campus. · The Opht ...
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Research Associate
3 weeks ago
Trust Co of West Los Angeles, United StatesPosition Summary · The Associate is a part of the Credit Research team within the Fixed Income Group. The Associate will work with experienced credit analysts to monitor positions and generate investment recommendations for our bank loan portfolios. The ideal candidate should hav ...
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Research Associate
16 hours ago
University of Southern California Los Angeles, United StatesUSC Department of Surgery recruiting a Research Associate. The Research Associate will plans, design and conduct highly technical and complex research projects independently and in consultation with division faculty. The Research Associate will also analyze research data, provide ...
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Research Associate
1 week ago
Insight Global Los Angeles, United StatesServe as a research associate for the Autism Intervention Research Network on Physical Health (AIR-P). The purpose of the AIR-P is to establish and maintain an interdisciplinary, multicenter research platform for scientific collaboration and infrastructure building. The Research ...
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Research Associate
21 hours ago
BioPhase Solutions Los Angeles, United StatesJob Description · Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Research Associate, Discovery Biology and Pharmacology to work for a leading Greater Los Angeles ...
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Research Associate
5 days ago
UCLA Outpatient Clinics Los Angeles, United States· The Semel Institute is seeking to hire a full time Staff Research Associate I to assist the project team in their aims to expand and improve the delivery of substance use disorder treatment. In this role you may also support the project team evaluating Californias Drug · Medi ...
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Research Associate
16 hours ago
Insight Global Los Angeles, United StatesMust Haves: · Bachelors degree and/or at least one year of professional work experience · Experience with research or following work processes (gathering requirements, capturing notes, documentation). Any clinical experience can work as well. · Customer service experience. Abi ...
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Research Associate
1 week ago
University of Southern California Los Angeles, United StatesResearch AssociateApply \_REQ /apply) Keck School of Medicine Los Angeles, California · AResearch Associateposition is available immediately in the Saito laboratory to study hepatic cell biology, hepatic inflammation, and innate antiviral immunology. Our laboratory utilizes the ...
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Research Associate
1 week ago
University of Southern California Los Angeles, United StatesResearch AssociateApply \_REQ /apply) Keck School of Medicine Los Angeles, California · AResearch Associateposition is available immediately in the Saito laboratory to study innate immunology against human pathogenic viruses and bacteria in the context of liver diseases. Our lab ...
Research Associate - Los Angeles, United States - Ampcus
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Description
SUMMARY STATEMENT The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies. The incumbent recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. The incumbent is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). 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.TYPE OF SUPERVISION RECEIVED This position assesses ongoing tasks and prioritizes assignments following established department/unit and research regulatory guidelines. Assignments will be given by the supervisor on a project basis, and the incumbent is expected to use his/her own judgment to accomplish tasks essential to research at a foundational level. The incumbent will seek guidance from direct supervisor to accomplish tasks of increased complexity for which there is not precedent. The incumbent will seek guidance from direct supervisor when there are conflicting demands. Work is reviewed in-progress or when deviating from standard procedures.
HOW LONG HAVE THE DUTIES & DISTRIBUTION OF TIME BEEN SUBSTANTIALLY AS BELOW?
ATTACH A COPY OF MOST RECENT ORGANIZATION CHART
AMOUNT OF
TIME
DUTIES AND TASKS % Administration/Clinical Research Coordinate research studies, identify participants according the IRB approved recruitment plan and assist the PI with determining patient eligibility. Facilitate the informed consent process, communicate protocol requirements to the participant, provide participant education related to protocol requirements and the significance of protocol compliance. Complete, organize and maintains all documentation required by the Food and Drug Administration (FDA) Code of Federal Regulations (CFR), Good Clinical Practice (GCP) Guidelines, or the funding source. Manages patient registration, data, and treatment assignment. Participates in quality control and quality assurance activities related to study workflows and documentation. Procure and distribute required study supplies to the appropriate sites for study start-up and ongoing study needs. Including Coordination of specimen collection, processing, & shipping biospecimens. Facilitate the safe and accurate completion of protocol required procedures in accordance with FDA CFR, GCP, and institutional best practice. Collect information for adverse event (AE) or serious adverse event (SAE) reporting to review with the Investigator and facilitates reporting requirements to applicable stakeholders (DSMB, IRB, funding source). % Data & Regulatory Management Assist in developing the study informed consent form(s) and amending the informed consent form(s) as applicable. Prepare and submit site or study-specific regulatory documents. Track and maintain required case histories/ essential documents as defined by FDA CFR and GCP to ensure regulatory compliance. Assist with routine and audits performed by internal review committees and/or external stakeholders. Ensure timely regulatory reporting and thorough documentation. Develops and implements adequate Corrective and Preventative Action (CAPA) plans as needed. % Training and Development Completes role-based training and occupational training as applicable, blood borne pathogens, infection control, hand hygiene, donning and doffing PPE. Attend study initiation meetings, and participate in team and general staff training events (, teleconferences, webcasts, and/or meetings). Completes protocol required training as needed. % Service Excellence Maintain a service centered approach for both internal and external, ensuring a high level of quality, communication, and support. Provide ongoing communication to all stakeholders to ensure pertinent information is disseminated. Timely response to and resolution of inquiries, both written and verbal, with the appropriate level of information for the request. Manage and resolve sensitive customer service related issues (internal/external stakeholders and patients). % Department Specific Responsibilities Manage all patient data within the EDC system (entry, queues, maintenance, and etc.). Perform pulmonary function testing in collaboration with pulmonary function research lab technicians. Work with the fund manager and purchaser on patient visit reimbursements and sponsor invoicing. Maintain regulatory and patient binders (on paper and electronically). Review electronic medical records to identify potential research participants. Other projects as assigned by supervisor and investigator. SKILLS, KNOWLEDGE AND ABILITIES TASK REFERENCE IMPORTANCE Bachelors Degree or - years of previous study coordination or clinical research coordination experience All Preferred Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborative relationships. All Essential Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness. All Essential Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment. All Required Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines. All Required Ability to respond to situations in an appropriate and professional manner. All Required Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines. All Required Ability to be flexible in handling work delegated by more than one individual. All Required Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications. All Required Ability to handle confidential material information with judgement and discretion. All Required Working knowledge of the clinical research regulatory framework and institutional requirements. All Preferred Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets. All Preferred Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research. All Preferred Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc. All Preferred Fluent in writing and speaking Spanish. All Preferred Demonstrated skills in using PC computer, MS Word, MS Excel, PowerPoint, Internet and Windows applications. All Preferred