169 Results for

Clinical Research Jobs in Oakwood, CA

Jobs

New!

Los Angeles, CAToday

$105,000–$115,000 Per Year

Key services include housing, mental health care, medical care, domestic violence services, substance abuse treatment, income assistance and life skills programs --- all aimed at improving the self-sufficiency of the individuals and families served. Day to Day Responsibilities: Attend meetings, respond to email correspondence, develop and maintain appropriate relationships (including with the Department of Mental Health and other Intensive Case Management support organizations) on behalf of the Senior Director and staff.

New!

Los Angeles, CAToday

$89,000–$100,000 Per Year

This role will oversee the IS PMO's most complex projects, which will likely involve a diverse set of components, including healthcare processes, clinical applications & interfaces, business / administrative applications & interfaces, enabling / supporting technology and infrastructure (e.g., hardware, devices, telecom, storage solutions). Information 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.

New!

Orange, CA3 days ago

$60,000–$72,000 Per Year

AHA Basic Life Support for Healthcare Professional (AHA BLS Healthcare) - American Heart Association; California Registered Nurse (RN) - CA Board of Registered Nursing; NIH Stroke Scale (NIHSS) - Various-Employee provides certificate; ACLS Certification (Advanced Cardiac Life Support) - American Heart Association--s-p-m1--. The stated pay scale reflects the range as defined by the collective bargaining agreement between Sharp HealthCare and Sharp Professional Nurses Network, United Nurses Associations of California/Union of Health Care Professionals, NUHHCE, AFSME, AFL-CIO.

New!

Orange, CA3 days ago

$60,000–$72,000 Per Year

New!

Los Angeles, CA3 days ago

$85,000–$102,000 Per Year

Duarte, CA13 days ago

City of Hope Medical Group provides a Permissive Time Away (PTA) program for eligible exempt employees, offering flexible paid time away for vacation, personal needs, and incidental illness without accrual limits. The Department of Medicine at City of Hope National Medical Center is seeking applications for a full-time clinical faculty and Hospital Epidemiology position (Assistant or Associate Clinical Professor) for our Duarte, California Campus.

Duarte, CA13 days ago

Opportunities for program growth include candidates with interests in graft versus host disease, cutaneous lymphoma, advanced skin cancers, adverse reactions to cancer treatment, and primary care dermatology for cancer survivors. The Department of Surgery, Division of Dermatology, is seeking two (2) dynamic, highly-qualified, board certified or eligible Dermatologist to meet the needs of our growing program in Southern California.

Irvine, CA13 days ago

By opening the new hospital – City of Hope’s second academic hospital in California – we are fulfilling our promise to Orange County and completing the continuum of care for people with cancer. Seeking research and mission-minded physicians who provide exceptional patient-centered care through clear communication and collaboration with members of the subspecialty teams.

Los Angeles30+ days ago

Remote

Responsibilities : 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.

Los Angeles, California30+ days ago

$70,304–$116,563 Per Year

Serves 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.

Los Angeles, California30+ days ago

$75,712–$129,792 Per Year

Orange, California17 days ago

Creating 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.

Whittier, CA30+ days ago

$27.44–$45.27

The 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.

Huntington Beach, CA30+ days ago

$55,000–$85,000 Per Year

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. 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.

Santa Clarita, CA30+ days ago

$60,000–$90,000 Per Year

Los Angeles, California30+ days ago

$21.06–$31.40

The 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.

Los Angeles, California12 days ago

$43,680–$65,062 Per Year

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. Posting Range: $43,680.00-$65,062.00 Location/Org Data : Closing: CHLA is a leader in pediatric and adolescent health, in our community, across the nation, and around the world .

Los Angeles, CA30+ days ago

Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. * Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE s and source documents.

Orange, California17 days ago

The 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.

Irvine, California28 days ago

$35.77–$36.54 Per Hour

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. Clinical research offices and clinics are located at the UCI Medical Center in Orange and the UCI campus in Irvine, as well as various clinics at community sites throughout Orange County.

Los Angeles, CA30+ days ago

$70,000–$100,000 Per Year

Due 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.

Irvine, CA30+ days ago

$30–$40 Per Hour

As 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).

Los Angeles, CA12 days ago

Full-time

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.

Irvine, California11 days ago

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. The Clinical Research Navigator works in close collaboration with Principal Investigators (PIs), Clinical Research Coordinators (CRCs), and other research support services to promote compliant and streamlined trial execution.

Huntington Beach, CA30+ days ago

$19–$33 Per Hour

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. The Clinical Research Assistantis an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.

Los Angeles, CA30+ days ago

Full-time

The 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.

Los Angeles, CA30+ days ago

$24–$38 Per Hour

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. The Travel Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.

Los Angeles, CA30+ days ago

Full-time

The Infusion Nurse is responsible for performing IV infusions of blinded and unblinded study drugs, obtaining blood specimens from participants, and maintaining accurate source documentation to uphold the integrity and reliability of clinical trial data. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research.

Los Angeles, CA30+ days ago

Part-time

The 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.

Los Angeles, CA30+ days ago

Part-time

Los Angeles, CA30+ days ago

Part-time

Los Angeles, CA30+ days ago

Part-time

Irvine, California18 days ago

Additionally, the incumbent is responsible for leading on-going training and education of CRCs, leading and managing pre-study site selection visits (PSSVs) including liaising with all appropriate ancilliary units (e.g., Investigational Drug Service, Pathology, Radiology, etc.) for the conduct of the trial, managing quality assurance and quality improvement goals and objectives through routine audit reviews of the team’s portfolio. The incumbent is also responsible for maintaining communication with all elements of a multi-level and multi-discipinary 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.

Whitter, CA30+ days ago

$52.50–$84.25

The clinical trial nurse is required to have comprehensive knowledge in all areas of protocol design, strong clinical assessment and decision-making skills, ability to navigate fast-paced hospital environments, manage multiple studies, excellent communication and patient education abilities, knowledge of federal regulations (FDA, OHRP), ICH-GCP guidelines, and HIPAA, proficient in EMRs and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). The fully integrated network is comprised of PIH Health Hospital - Whittier, PIH Health Hospital - Downey and PIH Health Good Samaritan Hospital, 27 outpatient medical locations, a multispecialty medical (physician) group, home healthcare services and hospice care, as well as heart, cancer, women’s health, urgent care and emergency services.

Los Angeles, CA30+ days ago

$34–$44 Per Hour

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. 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).

Los Angeles, CA30+ days ago

$34–$44 Per Hour

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. 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).

Orange, California30+ days ago

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. 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.

Northridge, CA30+ days ago

Full-time

Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of oncology, cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.

Irvine, CA30+ days ago

Full-time

Purpose: The Associate Director, Clinical Science & External Research (CSER) will drive end-to-end evidence generation and dissemination strategies (EGS/EDS) of scientific findings from clinical trials and postmarket studies sponsored by Johnson & Johnson MedTech Electrophysiology to generate clinical evidence for the company's pipeline that impacts patient lives. The ideal candidate for this position has proven success in the development of scientific communications and evidence dissemination plans in a medical device or related industry, is versed in supervising personnel writing and editing manuscripts, is knowledgeable of the cardiac arrhythmia medical device industry, and is familiar with pertinent regulations and guidelines governing clinical trial execution and clinical data publication.

Irvine, California30+ days ago

Listed among America’s Best Hospitals by U.S. News & World Report for 23 consecutive years, UCI Medical Center provides tertiary and quaternary care and is home to Orange County’s only National Cancer Institute-designated comprehensive cancer center, high-risk perinatal/neonatal program and American College of Surgeons-verified Level I adult and Level II pediatric trauma center, gold level 1 geriatric emergency department and regional burn center. *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.

Los Angeles, CA30+ days ago

Remote

Full-time

The Regional Recruitment Lead designs and executes regional enrollment strategies, ensures timely follow-up of all patient leads, and partners closely with corporate and site teams using a data-driven, hands-on leadership approach to consistently meet performance and revenue targets. Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines.

Irvine, CA30+ days ago

Key Responsibilities: • Support and organize the preparation of Clinical Study binders • Supervision of clinical study applications/submissions to Ethical Committees and Competent Authorities as an administrative support function to the Study Managers; • Support the Study Managers upon request from study managers based on project needs; • Responsible for all document archiving; • Control document validity and compliance (i.e. insurance certificates, etc.); • Organization of meetings related to clinical investigations such as Clinical Event Committees, Data Safety Monitoring Boards, Executive Committees and Steering Committees; • CTMS support • Support clinical department on all business needs • Organize and document (paper and LMS) together with Clinical Managers/Directors employees trainings and all internal meetings; • Manage all administrative aspects related to the Clinical Programs Europe THV in term of clinical study cost accountability; • Conduct payment overviews (cost lists and invoices) and issue payments upon request • Conduct periodic audits of documentation and may participate in internal master file audits • Provide coaching and training to lower level employees • Interact with clinical sites to resolve more complex device accountability issues • Provide training and technical support for internal and external users and set-up of new users in Wavemark • Strict attention to detail • Ability to interact professionally with all organizational levelsEducation:Education and Experience: H.S. Diploma or equivalent 6 years experience previous related experience Required Additional Skills: • Proven expertise in MS Office Suite, Adobe, and ability to operate general office machinery • Experience with an ERP software, JDE and CTMS (Clinical Trial Management System) preferred • Excellent written and verbal communication skills and interpersonal relationship skills • Ability to work in a fast paced environment • Demonstrated problem-solving and critical thinking skills.

Orange, California17 days ago

$27.40–$34.43 Per Hour

The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and . In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI).

Los Angeles, California11 days ago

$57,949–$95,202 Per Year

Purpose Statement/Position Summary: The Health Science & Behavioral Research Associate I is under the supervision of the Research Associates/Research Managers, will assist the PI Dr. Jessica Schwartzman in coordinating research studies including participant recruitment, scheduling study visits, data collection (e.g., clinical interviews, EEG tasks, eyetracking tasks, surveys), data entry and maintenance using REDCap, and/or study documentation. 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.

Los Angeles, California30+ days ago

$70,304–$99,341 Per Year

The individual should be able to work independently to coordinate and manage consortium activities at the central operations center, with guidance from the appointed consortium leaders (e.g., Consortium Medical Director, Associate Medical Director, Administrative Director, etc.). Clinical trial experience includes but is not limited to study protocol development, regulatory maintenance, and reporting (e.g., SAEs, IRB submissions, etc.), eCRF development, data management, and coordination of investigational product.

Orange, California17 days ago

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. The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, 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.

Los Angeles, California25 days ago

$70,304–$110,573 Per Year

Responsibilities include, but are not limited to: participant recruitment, enrollment, and retention; conducting research assessments; managing research databases (e.g., REDCap); tracking study progress; ensuring data quality and regulatory compliance; maintaining accurate records and confidentiality in accordance with study protocols and institutional guidelines. Purpose Statement/Position Summary: Under the supervision of the Research Associates/Research Managers, the Health Science & Behavioral Science Research Associate II recruits project participants and administers structured and/or interview survey materials.

Los Angeles, California13 days ago

$43,680–$61,953 Per Year

Applicants should have experience in: Bacterial cell culture, Mammalian cell culture, PCR, Restriction Enzyme Digestion, Plasmid DNA Purification, Immunofluorescence Staining, Western Blot, In Vitro Mutagenesis, Long-Term Killing Assay, ELISA, Flow Cytometry (FACS), Dual Luciferase Assay, Transfection, Transformation, Plasmid DNA amplification, Mice Handling, Euthanasia Competency, Intraperitoneal Injection, Mice Necropsy, Cellular Reprogramming, Microsoft Word, Excel, and PowerPoint. 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.

Santa Monica, California9 days ago

£82,135–£102,683

Perform routine laboratory procedures including ddPCR, qPCR, Flow, Luminex/MSD for ELISA and various cell-based immunoassays and biochemical assays. R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering.

Los Angeles, CA30+ days ago

$43,680–$61,953 Per Year

The Associate Research Specialist will perform basic molecular biology work, including but not limited to DNA extraction/isolation, PCR, gel electrophoresis, sequencing prep, RNA extraction, qRT-PCR, protein extraction/quantification, enzyme assays, cell culture, and microscopy/imaging. Education/Licensure/Certification: A Bachelors’ degree, in a related scientific field (e.g., biology, microbiology, biochemistry, chemistry, engineering) Applicants must have completed their Bachelor’s degree by their anticipated start date.

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Clinical Research Jobs in Oakwood, CA

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Clinical SupervisorJobot

Healthcare IT Training SpecialistJobot

Clinical Nurse RN - Neuroscience ICU - Sharp Grossmont Hospital - Night - Full-time - Eligible for up to $10K in New Hire Incentives -Relocation Bonus 5000SHARP HEALTHCARE

Clinical Nurse RN - Neuroscience ICU - Sharp Grossmont Hospital - Night - Full-time - Eligible for up to $10K in New Hire IncentivesSHARP HEALTHCARE

Clinical Nurse RN - Neuroscience ICU - Sharp Grossmont Hospital - Night - Full-time - Eligible for up to $10K in New Hire Incentives - Relocation Bonus 5KSHARP HEALTHCARE

Physician | Infectious Diseases | Duarte, CACity of Hope

Physicians| Dermatologists | City of Hope (CA)City of Hope

Physician| Neurologist | Irvine, CACity of Hope

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA)Medpace, Inc.

Clinical Research Coordinator IIChildren's Hospital Los Angeles

Clinical Research Coordinator IIIChildren's Hospital Los Angeles

Clinical Research CoordinatorUniversity of California, Irvine

Clinical Research Coordinator, Full time, DaysPIH Health

Clinical Research Coordinator I (Huntington Beach, CA)Care Access

Clinical Research Coordinator IICare Access

Experienced Clinical Research CoordinatorGreater Los Angeles Veterans Research and Education Foundation

Clinical Research AssistantChildren's Hospital Los Angeles

Clinical Non-Licensed Pool/Clinical Research CoordinatorDiverse Linx

Asst. Clinical Research Coordinator - HybridUniversity of California, Irvine

Temporary Clinical Research Coordinator (CRC)University of California, Irvine

Travel Clinical Research CoordinatorCare Access

Clinical Research CoordinatorWake Research

Clinical Research Coordinator (Oncology)Flourish Research

Clinical Research NavigatorUniversity of California, Irvine

Clinical Research AssistantCare Access

Clinical Research Assistant (Pre-Medical Track) Must Speak English and SpanishAngel City VA

Travel Clinical Research AssistantCare Access

Clinical Research Oncology NurseFlourish Research

Clinical Research Assistant (Must Live in Los Angeles and Speak Spanish)Angel City VA

Clinical Research Assistant (Must live in Los Angeles and Speak Spanish)Angel City VA

Clinical Research AssistantAngel City VA

Clinical Research Assistant Must Be Bilingual English-SpanishAngel City VA

Clinical Research Manager - HybridUniversity of California, Irvine

RN Clinical Research, Full time, 8am-4:30pmPIH Health

Clinical Research Assistant, PRNCare Access

Clinical Research Assistant, PRN (Bilingual - Registered Nurse)Care Access

Clinical Research ManagerUniversity of California, Irvine

Clinical Research AssistantFlourish Research

Associate Director, Clinical Science & External Research (Electrophysiology) - MedTechJohnson and Johnson

Medical Assistant/Admit Worker - Center for Clinical Research - FT DaysUniversity of California, Irvine

Regional Patient Recruitment Lead - Clinical ResearchFlourish Research

Sr. Clinical Research RepresentativeOQSIE

ASST. RESEARCH DATA COORDINATOR - HYBRIDUniversity of California, Irvine

Health Science & Behavioral Research Associate IChildren's Hospital Los Angeles

Coordinator, Clinical Trial OperationsChildren's Hospital Los Angeles

Research Data Coordinator - HybridUniversity of California, Irvine

Health Science & Behavioral Research Associate IIChildren's Hospital Los Angeles

Associate Research SpecialistChildren's Hospital Los Angeles

Research Associate - Biology IIRD Partners

Associate Research Specialist / HemOnc / Full-time / Dr. Kuo LabChildren's Hospital Los Angeles

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