JobotNewClinical Research Coordinator (Contract) JobotClinical Research Coordinator (Contract)Anaheim, CA$33–$36 / hourInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. The Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
Orange County Neuropsychiatric ReseClinical Research Coordinator - Entry-Level Orange County Neuropsychiatric ReseClinical Research Coordinator - Entry-LevelLos Angeles, CAThe CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research colleagues and departments. We specialize in pharmaceutical clinical trials involving CNS (Central Nervous System) disorders such as Schizophrenia, Bipolar Disorder, Depression, ADHD, Autism, and more.
ApexFocusGroupPart-Time/Full-Time Research Panel. Entry Level. Receptionist or Typist Welcome ApexFocusGroupPart-Time/Full-Time Research Panel. Entry Level. Receptionist or Typist WelcomeAnaheim, CARemote$15,000–$36,000We’re inviting individuals from all backgrounds, including those searching for entry level positions, such as, receptionist or typist roles, to express interest in joining upcoming consumer research studies. Research formats vary and may include focus groups (remote online or in-person), video interviews, product evaluations, or digital feedback sessions .
Anaheim Clinical Trials, LLCData Entry - Clinical Research Anaheim Clinical Trials, LLCData Entry - Clinical ResearchAnaheim, CA$20–$21 / hourPart timeAssist CRCs in entering data from paper source documents to eCRFs correctly, accurately and on a timely manner for multiple clinical trials. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Workoo TechnologiesNewData Entry Clerk Needed , Entry Level (Remote) Workoo TechnologiesData Entry Clerk Needed , Entry Level (Remote)Los Angeles, CARemoteDevelop, sustain, and also build scalable records pipelines and also records architectureTake advantage of data narration concepts to create clear and also impactful data visuals images making use of Electrical power BIHelp automate existing business functions and also boost exception-based coverageDeal with IT and also BA's to check out, study, as well as get brand new records variables (data exploration).Analyze big datasets to identify purposeful patterns that give workable end results. Strong experience collaborating with PowerBI.Servicing various disclosing items like Sizes, Measures, Filters, Calculated Area, changes, specifications, relative format, DAX queries, Communications, etc in Electrical power BI.Understanding of DAX, SQL, M Code.
Regal Executive SearchTax Accountant - Entry Level Regal Executive SearchTax Accountant - Entry LevelSherman Oaks, CAOther responsibilities include assisting the Senior Manager and Partner with tax projections, research, and various other miscellaneous tax related projects. Our client base includes high net worth individuals and their related companies with a focus on entertainment.
NoGigiddyEntry-Level Remote Sales Development Representative (20 - 27 per hour) NoGigiddyEntry-Level Remote Sales Development Representative (20 - 27 per hour)Los Angeles, CARemote$41,600–$56,160Account Coordination: Assist in coordinating client accounts, including setting up new accounts, managing renewals, and ensuring all client information is up to date. Client Relationship Management: Build and maintain strong relationships with clients, understanding their needs and ensuring their satisfaction.
Recruit MonitorNewRemote Data Entry Operator / Entry Level Recruit MonitorRemote Data Entry Operator / Entry LevelLos Angeles, CARemoteNeeded AbilitiesMust maintain an overall understanding of policies and also techniquesHave strong interpersonal capabilities utilizing tact, persistence and politenessMaintain the capacity to collect, research study, arrange and analyze dataHave the capacity to work as an employee, however additionally individually sometimes with limited instructionsProductive at the office in a fast-paced environmentPreserve flexibility and/or the ability to burn the midnight oil as needed to have to meet rigid schedules and planCalled for ExpertiseSenior High School Degree or comparable called forMust have Private location to function and room to set-up devices and also High Speed Net connectionAdvantagesJob From House ! EMG staff members appreciate a vast array of perks including: On-the-Job Instruction.#J-18808-Ljbffr.
Marcus & MillichapEntry-Level Commercial Real Estate Agent - Encino Marcus & MillichapEntry-Level Commercial Real Estate Agent - EncinoEncino, CAWe focus on bringing together specialized market knowledge, the industry's leading brokerage platform and exclusive access to inventory to achieve exceptional results for our clients, year after year. Our mission is to help our clients create and preserve wealth by providing the best real estate investment sales, financing, research, and advisory services available.
Marcus & MillichapEntry-Level Commercial Real Estate Agent Marcus & MillichapEntry-Level Commercial Real Estate AgentLos Angeles, CAWe focus on bringing together specialized market knowledge, the industry's leading brokerage platform and exclusive access to inventory to achieve exceptional results for our clients, year after year. Our mission is to help our clients create and preserve wealth by providing the best real estate investment sales, financing, research, and advisory services available.
KPFF Consulting EngineersNewEntry Level Structural Designer KPFF Consulting EngineersEntry Level Structural DesignerIrvine, CA$80,000–$90,000 / yearKPFF is looking for full-time structural engineering professionals who are self-motivated and eager to deepen their knowledge of structural engineering while gaining real-world experience. KPFF is proud to provide our employees with benefits options that fit their unique lives, including: Medical insurance options to choose from, VSP Vision Insurance, and Delta Dental Insurance.
Cargo Express FreightEntry level Sales - Logistics Cargo Express FreightEntry level Sales - LogisticsAnaheim, CA$35,000–$45,000With the best technology and know-how in the industry we're not just moving freight—we're building lasting partnerships with clients across the country. Cargo Express Freight is a fast-growing, asset-based logistics company built on reliability, innovation, and unmatched customer service.
Sparkbit 360Entry Level Marketing Agent Sparkbit 360Entry Level Marketing AgentLos Angeles, CaliforniaAs an Entry Level Marketing Agent, you will be exposed to a wide range of marketing activities, including digital campaigns, market research, client communications, and content creation. As a full-service marketing and public relations agency, we are dedicated to helping businesses thrive through meaningful connections, strategic planning, and impactful experiences.
Pacific Neuropsychiatric Specialists IncClinical Research Assistant Pacific Neuropsychiatric Specialists IncClinical Research AssistantOrange, CAUnder policy direction from the Practice Manager and Lead Coordinator, and with the support of the COO, the Clinical Research Assistant will play a crucial role in supporting clinical research activities, ensuring adherence to protocols, and contributing to the advancement of medical knowledge. The Clinical Research Assistant is responsible for drawing blood, performing lab tests, scheduling patients, tracking patient data and performing other clerical duties for the office.
Angel City VAClinical Research Assistant Angel City VAClinical Research AssistantLos Angeles, CAPart timeThe Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
Angel City VAClinical Research Assistant (Must live in Los Angeles and Speak Spanish) Angel City VAClinical Research Assistant (Must live in Los Angeles and Speak Spanish)Los Angeles, CAPart timeThe Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
Angel City VAClinical Research Assistant (Must Live in Los Angeles and Speak Spanish) Angel City VAClinical Research Assistant (Must Live in Los Angeles and Speak Spanish)Los Angeles, CAPart timeThe Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
Angel City VAClinical Research Assistant Must Be Bilingual English-Spanish Angel City VAClinical Research Assistant Must Be Bilingual English-SpanishLos Angeles, CAPart timeThe Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
HITEJINRO AMERICASales Manager Entry Level HITEJINRO AMERICASales Manager Entry LevelLA PALMA, CAThe Sales Manager Entry Level develops and maintains strong relationships with new and existing distributors and control state agencies, providing products and strategic support to build and grow a successful brand portfolio. Established in 1924, HiteJinro has over 100 years of heritage and is recognized globally for its iconic green bottle and leadership in Korean drinking culture.
HITEJINRO AMERICASales Manager_Entry Level HITEJINRO AMERICASales Manager_Entry LevelLA PALMA, CA$70,000–$73,000 / yearThe Sales Managing Associate develops and maintains strong relationships with new and existing distributors, providing products and strategic support to build and grow a successful brand portfolio. Established in 1924, HiteJinro has over 100 years of heritage and is recognized globally for its iconic green bottle and leadership in Korean drinking culture.
Angel City VAClinical Research Assistant (Pre-Medical Track) Must Speak English and Spanish Angel City VAClinical Research Assistant (Pre-Medical Track) Must Speak English and SpanishLos Angeles, CAFull timeThe Clinical Research Assistant (CRA) is an entry-level, pre-professional role designed for pre-medical or health-sciences students seeking structured exposure to clinical research and patient-facing clinical environments. This role does not include independent study coordination or regulatory decision-making responsibilities and functions under close supervision at all times.
Anaheim Clinical Trials, LLCNewMedical Assistant - Clinical Research Anaheim Clinical Trials, LLCMedical Assistant - Clinical ResearchAnaheim, CA$20–$21 / hourPart timeProvides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
University of California, IrvineClinical Research Manager University of California, IrvineClinical Research ManagerOrange, CaliforniaMisconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. Responsibilities: Under the general direction of the Assistant Director of Clinical Research Operations of the UCI Center for Clinical Research (CCR), the Clinical Research Manager (CRM) is responsible for all clinical research operational matters in fulfilling the mission of CCR under the University of California Irvine School of Medicine and the overall UC Irvine Health enterprise.
Clinical Innovation Inc.Medical Assistant - Clinical Research Clinical Innovation Inc.Medical Assistant - Clinical ResearchBellflower, CA$20–$22.50 / hourPart timeProvides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
Clinical Innovation Inc.Medical Assistant - Clinical Research (6:00 pm - 6:00 am) Clinical Innovation Inc.Medical Assistant - Clinical Research (6:00 pm - 6:00 am)Bellflower, CAPart timePreparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Collaborative Neuroscience Research, LLCMedical Assistant - Clinical Research Collaborative Neuroscience Research, LLCMedical Assistant - Clinical ResearchTorrance, CA$20–$22.50 / hourPart timeProvides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
Medpace, Inc.Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA) Medpace, Inc.Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA)Los AngelesRemoteResponsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.
Wake ResearchClinical Research Coordinator Wake ResearchClinical Research CoordinatorIrvine, CA$30–$40 / hourAs of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data. M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs).
CIBDResearch Assistant CIBDResearch AssistantOrange, CACIBD is the regional grantee for the Western States Region for Hemophilia, the Pacific Sickle Cell Regional Collaborative (PSCRC) and Networking California for Sickle Cell Care (NCSCC) providing regional leadership, fiscal and administrative oversight, grants management, capacity building, clinical education, technical assistance, evaluation, and outreach to public and private health agencies at the local, state, and federal levels. CIBD is a part of a nationwide network of over 140 Hemophilia Treatment Centers that use multidisciplinary teams of blood disorder specialists to provide expert comprehensive diagnosis, medical care, outreach, education, outcomes monitoring, surveillance, and prevention services to people with Hemophilia, Sickle-Cell Anemia, Thalassemia, Von Willebrand Disease, Mast Cell Activation Syndrome (MCAS) and other related benign hematology conditions.
Care AccessClinical Research Assistant, PRN (Bilingual - Registered Nurse) Care AccessClinical Research Assistant, PRN (Bilingual - Registered Nurse)Los Angeles, CA$34–$44 / hourWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).
Care AccessClinical Research Assistant, PRN Care AccessClinical Research Assistant, PRNLos Angeles, CA$34–$44 / hourWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).
Charles R. Drew University of Med & ScClinical Research Program Manager Charles R. Drew University of Med & ScClinical Research Program ManagerLos Angeles, CA$75,700–$90,000 / yearPart timeThe Clinical Research Program Manager works closely with the Director, Principal Investigators (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to manage the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Ability to develop and maintain professional working relationships in complex program/organizational settings involving heterogeneous constituents such as academic and clinical faculty, staff, students, and community partners from diverse backgrounds.
Charles R. Drew University of Med & ScResearch Assistant Professor Charles R. Drew University of Med & ScResearch Assistant ProfessorLos Angeles, CAPart timeWorks with investigators to formalize analysis plans and reporting specifications; advises as to choice of statistical analysis strategies, reliability of measurements and identifiability of models, and interpretation and presentation of statistical results. Builds and sustains collaborative relationships with individuals in different disciplines and serves as subject-matter expert for research teams, internal and external committees, and other constituencies and collaborators.
Anaheim Clinical Trials, LLCClinical Research - Regulatory Specialist Anaheim Clinical Trials, LLCClinical Research - Regulatory SpecialistAnaheim, CA$30–$35 / hourPart timeCollects, prepares, and submits documentation to various sponsors/CROs during study start-up, including: Submission documents/approval, Protocol amendments with respective signature pages, Informed consent documents, FDA form 1572, Lab normal result documents, financial disclosure forms, Delegation of authority logs, Licenses, Reports. With moderate oversight the Regulatory Coordinator I is responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiation, execution, and reporting on the various status of research tasks in accordance with FDA guidelines, ICH GCP and SOPs.
Care AccessTravel Clinical Research Coordinator Care AccessTravel Clinical Research CoordinatorLos Angeles, CA$70,000–$100,000 / yearDue to enhanced experience in Care Access' decentralized clinical research process, the Travel Clinical Coordinator will be able to assume a greater study workload, overall study responsibility, and more detailed, Site, Sponsor and CRO interactions, while conveying a positive image of Care Access to the community, Sponsors, CROs, and study participants and their family members. With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress.
Greater Los Angeles Veterans Research and Education FoundationExperienced Clinical Research Coordinator Greater Los Angeles Veterans Research and Education FoundationExperienced Clinical Research CoordinatorLos Angeles, California$21.06–$31.40The CRC supports multiple Phase II-IV clinical trials across a variety of disciplines and investigators which may be sponsored by federal agencies including NIH or DOD and pharmaceutical sponsors or CRO’s. Schedule and attend all Site Initiation Visits, Monitoring Visits, Close-Out Visits etc. for all assigned studies/or when asked to attend by the Lead Clinical Coordinator.
University of California, IrvineTemporary Clinical Research Assistant University of California, IrvineTemporary Clinical Research AssistantOrange, CaliforniaMisconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. Enter and manage patient and study information in electronic databases and the Clinical Trial Management System (OnCore), while supporting research coordinators and managers with study logistics and administrative tasks.
Career Launch AIPublic Equity Research Analyst Career Launch AIPublic Equity Research AnalystLos Angeles, CA$100,000–$120,000A leading investment bank is seeking an Equity Research Analyst to support coverage of a high-growth sector (Tech, Healthcare, Industrials, Consumer, or TMT). You will learn how to analyze companies, markets, and financials in depth while supporting institutional clients.
Career Launch AIEquity Research Analyst Career Launch AIEquity Research AnalystLos Angeles, CA$100,000–$120,000A leading investment bank is seeking an Equity Research Analyst to support coverage of a high-growth sector (Tech, Healthcare, Industrials, Consumer, or TMT). You will learn how to analyze companies, markets, and financials in depth while supporting institutional clients.
Care AccessClinical Research Coordinator II Care AccessClinical Research Coordinator IISanta Clarita, CA$60,000–$90,000 / yearWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
University of California, IrvineClinical Research Coordinator University of California, IrvineClinical Research CoordinatorOrange, CaliforniaCreating a center of excellence for cell-based therapeutics that addresses the unique challenges of testing and delivering novel cell therapies by integrating and building upon the extensive experience and many strengths of UCLA, UCI, and our partners; 2. Building interactive and highly trained teams and electronic data sharing systems to accelerate and translate discovery to improve human health; 3. Transforming the delivery of cell therapeutics through our proven Good Manufacturing Practice (GMP) manufacturing; 4. Advancing, expanding, and integrating educational opportunities to inform patients, families, communities, and clinicians of the full range of scientifically sound and medically appropriate, regulated stem cell-based clinical trials while providing objective information about potentially dangerous and unproven procedures; 5. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
22nd Century Technologies, Inc.Non-Clinical - Administrative - Clinical Research Assistant 22nd Century Technologies, Inc.Non-Clinical - Administrative - Clinical Research AssistantLos Angeles, CAUnder the supervision and direction of the Chief of Anatomic Pathology, and/or Director of Operations, Anatomic Pathology, and/or the Clinical Specialist Supervisor, the Clinical Specialist (Pathologists' Assistant) provides support to the Anatomic Pathology Department. 2. Completion of a NAACLS-Accredited PA Program: You must successfully complete a Pathologists' Assistant program accredited by the NAACLS (National Accrediting Agency for Clinical Laboratory Sciences).
Anaheim Clinical Trials, LLCPatient Recruitment - Research Assistant (Bilingual Mandarin) Anaheim Clinical Trials, LLCPatient Recruitment - Research Assistant (Bilingual Mandarin)Anaheim, CA$20–$22 / hourPart timeResponsible for recruiting patients over the phone as well as assisting with recruitment programs to increase referrals of participants for the various clinical research trials. . We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
University of California, IrvineClinical Research Coordinator - Hybrid University of California, IrvineClinical Research Coordinator - HybridOrange, CaliforniaThe incumbent is also responsible for maintaining communication with all elements of a multi-level research network, including attending Disease Oriented Teams (DOTs) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
University of California, IrvineAsst. Clinical Research Coordinator - Hybrid University of California, IrvineAsst. Clinical Research Coordinator - HybridOrange, CaliforniaThe incumbent is also responsible for maintaining communication with all elements of a multi-level research network, including attending Disease Oriented Teams (DOTs) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
Children's Hospital Los AngelesClinical Research Coordinator II Children's Hospital Los AngelesClinical Research Coordinator IILos Angeles, California$70,304–$116,563 / yearServes as a resource for study team members and principal investigators and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Children’s Hospital Los Angeles is consistently ranked among the top 10 children's hospitals in the nation, delivering world-class care through more than 350 specialized programs and services.
Orange County Neuropsychiatric ReseClinical Research Coordinator - Experienced Orange County Neuropsychiatric ReseClinical Research Coordinator - ExperiencedLos Angeles, CAWe specialize in pharmaceutical clinical trials involving Central Nervous System disorders such as Schizophrenia, Bipolar Disorder, Depression, ADHD, Autism and numerous medical indications in Rheumatology and Vaccine development. The CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research colleagues and departments.
University of California, IrvineSR. CLINICAL RESEARCH COORDINATOR - HYBRID University of California, IrvineSR. CLINICAL RESEARCH COORDINATOR - HYBRIDOrange, CaliforniaThe incumbent is also responsible for maintaining communication with all elements of a multi-level research network, including attending Disease Oriented Teams (DOTs) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
Ultimate Staffing ServicesMarket Research Assistant Ultimate Staffing ServicesMarket Research AssistantIrvine, California$25–$25 / hourConduct basic vetting of accounts to determine whether the business sells supplements, appears to offer private label products, carries competitive brands, and the general size or profile of the store. Prior experience in research, data entry, lead generation, administrative support, sales support, or account/prospect research preferred.
PIH HealthClinical Research Coordinator, Full time, Days PIH HealthClinical Research Coordinator, Full time, DaysWhittier, CA$27.44–$45.27The fully integrated network is comprised of PIH Health Downey Hospital, PIH Health Good Samaritan Hospital, PIH Health Whittier Hospital, 37 outpatient medical office buildings, a multispecialty medical (physician) group, home healthcare services and hospice care, as well as heart, cancer, digestive health, orthopedics, women’s health, urgent care and emergency services. The organization is nationally recognized for excellence in patient care and patient experience, and the College of Healthcare Information Management Executives (CHIME) has identified PIH Health as one of the nation’s top hospital systems for best practices, cutting-edge advancements, quality of care and healthcare technology.