136 Results for

Clinical Research Jobs in Orange, CA

Jobs

New!

Newport Beach, CA3 days ago

$52–$75

Job OverviewWe are actively seeking a Clinical Research Coordinator RN II to join a leading healthcare organization at Hoag. This is an excellent opportunity for an experienced RN with a background in clinical research, especially in advanced therapies such as cell therapy and CAR-T.

Irvine, CA7 days ago

$30–$35 Per Hour

Identify, develop, recommend, and implement process development and improvement solutions to optimize global trial workflow. Produce daily/weekly/monthly reports as well as ad hoc requests to be fulfilled by the operations team.

New!

Irvine, CA1 day ago

$30–$35 Per Hour

Coordinate with cross-functional teams including Clinical, Supply Chain, Manufacturing, Finance, and Quality . If you think this Clinical Operations Specialist position is a good fit for you, please reach out to me - feel free to call, e-mail, or apply to this posting!

New!

Fountain Valley, CA2 days ago

$19–$22 Per Hour

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. You will utilize your medical reception skills to provide outstanding service while coordinating patient flow, managing appointments, and maintaining accurate patient records.

New!

Corona, CA2 days ago

$26–$29 Per Hour

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. A prominent oncology network has a Riverside clinic that is seeking a polished, patient-first Non-Clinical Medical Assistant/Office Supervisor to own the front-office experience and keep daily operations running smoothly.

New!

Orange, CA5 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, CA5 days ago

$60,000–$72,000 Per Year

New!

Los Angeles, CA5 days ago

$85,000–$102,000 Per Year

New!

Tustin, CA1 day ago

Temporary

This role will be responsible for managing the full lifecycle of contracts related to clinical trials, vendors, and strategic partnerships, ensuring compliance with regulatory requirements and company policies. We are seeking a detail-oriented and highly organized Contracts Administrator to support our growing biopharmaceutical operations.

New!

West Hollywood, CAToday

$350,000–$400,000 Per Year

The Chief of the Cardiology Division at VA Greater Los Angeles Healthcare System (VAGLAHS) will lead and oversee all aspects of cardiology care, education, research, and mentorship in a dynamic academic and clinical environment. Provide expertise and direct patient care in non-invasive and/or invasive cardiology (including echocardiography, TEE, nuclear cardiology, stress testing, electrophysiology, and/or cardiac catheterization).

New!

Duarte, CA1 day 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.

New!

Duarte, CA1 day 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.

New!

Irvine, CA1 day 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.

Newport Beach, CA30+ days ago

Contractor

Job Title: Registered Nurse (RN) - Clinical Research Coordinator II Job Location: Newport Beach, CA Job Duration: 2-3 Months (possibility of extension) Job Summary: The Clinical Research Coordinator-Registered Nurse II (CRC RN-II) is responsible for all aspects of clinical research activities and works in close cooperation with study physicians, inter- and intradepartmental stakeholders, and sponsors. Job Responsibilities: Manages complex clinical research trials including industry-sponsored, government-funded, and investigator-initiated studies.

Orange, California19 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.

New!

Orange, California1 day 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.

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.

New!

Newport Beach, CA6 days ago

Responsibilities:Manages complex clinical research trials including industry-sponsored, government-funded, and investigator-initiated studies. Accurately collects, records, and enters study data into clinical research databases while maintaining data integrity and quality.

Newport Beach, CA30+ days ago

The Clinical Research Coordinator-Registered Nurse II (CRC RN-II) is responsible for all aspects of clinical research activities and works in close cooperation with study physicians, inter- and intradepartmental stakeholders, and sponsors. Excellent verbal and written communications and presentation skills; excellent organizational skills; close attention to detail and excellent interpersonal skills to work effectively in a diverse team.

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.

Orange, California19 days ago

Irvine, California30 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.

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).

Irvine, California13 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.

Irvine, California20 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.

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.

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.

New!

Orange, California1 day 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 Department of Radiological Sciences is dedicated to conducting leading-edge research, providing the highest quality clinical education and delivering state-of-the-art care to our patients through the advanced diagnosis and treatment of disease through biomedical research.

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, California19 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).

Orange, California19 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.

Mission Viejo, CA30+ days ago

$110,000–$145,000 Per Year

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 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).

New!

San Juan Capistrano, CA1 day ago

The Director, Quality sits as a member of the Business Unit's Leadership Team and is responsible for participating in all associated communications, planning and coordination activities and works closely with Managing Director-Operations/Business/Staffing. Identify and relate the quality control, quality management requirements of Quest Diagnostics Inc. and the State, Federal and other agencies to department directors, managers, and supervisors to ensure that these requirements are implemented and auditd .

New!

Duarte, CA1 day ago

$78–$124 Per Hour

Pharmacy Practice Residency (PGY 1) and Hematology/Oncology Specialty Residency (PGY2), or Five years of experience as a clinical pharmacist in a research or hematology/oncology or other specialty settings with exposure to investigational studies, may substitute for the required residencies, or A PGY1 residency plus three years of experience as a clinical pharmacist in a research or hematology/oncology or other specialty setting with exposure to investigational studies may substitute for the required PGY2 residency. The Investigational Drug Services (IDS) Clinical Pharmacist Specialist (CPS) independently supports pharmaceutical care services and the growth of the clinical research program through collaboration with Pharmacy and Research leadership, sponsors, regulatory agencies, investigators, and multidisciplinary care teams.

Irvine, California7 days ago

Remote

$61,050–$77,000 Per Year

Overview: Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. This role assists the invoicing process throughout the different stages of clinical trials and interacts with healthcare professionals and internal project teams and accounts payable (AP).

Orange, CA8 days ago

The Field Clinical Specialist will provide comprehensive clinical, technical, and educational support to ensure the safe and effective use of our leadless left ventricular (LV) Cardiac Resynchronization Therapy (CRT) devices. Willingness to travel approximately 80% of the time to various locations, including but not limited to healthcare facilities, industry events, and office(s), with frequent travel to healthcare facilities within the assigned territories (may include weekends, overnight, and international travel).

Irvine, CA23 days ago

G., clinical study teams, Manufacturing Operations, Finance, Supply Chain, Quality, and Compliance groups) to develop and lead the execution of the device process, and ensuring continuous process improvement of efficiency and accuracy of processes and procedures. Review and ensure accuracy and completeness of clinical study files, enter into computerized tracking system, and file/scan for archive, for multiple clinical research trials .

Irvine, California30+ days ago

New!

Orange, CA1 day ago

$220,000–$289,940 Per Year

The UCI Neurology Movement Disorders Program offers comprehensive, compassionate, world-class care for the spectrum of adult movement disorders, including Parkinson's disease; essential tremor; Lewy Body disease; Huntington's disease as a HDSA Center of Excellence; dystonia; tic disorders; chorea; myoclonus; and atypical parkinsonism. We benefit from cross-cutting collaborations with leading scientists on campus, including UCI MIND and the ADRC, and the patient experience is enhanced by our working closely with colleagues across a number of departments, such as the Neurosurgery, Family Medicine/Geriatric Medicine and Gerontology, and the Susan Samueli Integrative Health Institute.

Ontario, California15 days ago

$138,230.12–$200,406.07 Per Year

Contacts, develops new and maintains established clinical affiliations, assuring all clinical sites meet the program’s prescribed learning outcomes, and securing appropriate contact and specific contractual agreement information including identified preceptors, number and types of placements, renewals, insurance and liability matters, and other pertinent issues important to seamless transition of students to clinical sites. During the development phase of the program, primary responsibilities include clinical site development, assuring clinical sites meet the program’s prescribed expectations for student learning and performance evaluation, oversight of affiliation agreements, planning and coordinating clinical faculty development, curricular development, and oversight of clinical year scheduling.

Irvine, CA23 days ago

Ensure compliance with regulations and manage the lifecycle of devices, while closely partnering with other internal key stakeholders ( e.g., clinical study teams, Manufacturing Operations, Finance, Supply Chain, Quality, and Compliance groups) to develop and lead the execution of the device process, and ensuring continuous process improvement of efficiency and accuracy of processes and procedures. Job Description: Identify, develop, recommend, and implement, moderately complex process development and process improvement solutions to optimize global trial workflow timelines, (e.g., device return aging issues, status of open device issues/queries, etc.).

Costa Mesa, CA30+ days ago

Contractor

Review and resolve discrepancies in Oncology data in conjunction with Supervisor of Oncology Data, physician team, and other clinical data staff. Work Schedule: M-F set days, some flexibility with hours but traditional 8 hour day shift starting around 8-9am and 4:30-5pm.

New!

Irvine, CA5 days ago

$100,000–$200,000 Per Year

The ideal candidate will have hands-on experience creating QC systems for, developing, validating, and troubleshooting immunoassays for clinical or research applications, with a strong understanding of assay performance characteristics, reagent development, and analytical methods. The selected candidate will be responsible for: Design, develop, optimize, and validate immunoassays for automated platforms including Phadia and/or IMMULITE systems.

Costa Mesa, CA30+ days ago

For URAC accredited areas, the following professional competencies apply: Associates in this role are expected to have strong oral, written and interpersonal communication skills, problem-solving skills, facilitation skills, and analytical skills. + Unless expressly allowed by state or federal law, or regulation, must be located in a state or territory of the United States when conducting utilization review or an appeals consideration and cannot be located on a US military base, vessel or any embassy located in or outside of the US, unless they are command-sanctioned activities.

Irvine, CA30+ days ago

$106,000–$125,000 Per Year

Moderate knowledge and understanding of the following areas including valve crimping, case management, pre-case planning, post case management, Therapy Awareness Program management, and clinical education programs. Our Implantable Heart Failure Management (IHFM) team is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention.

Whittier, CA30+ days ago

$130,000–$140,000

The PD works with the Executive Dean of the College of Chiropractic Education (ED) on program and teaching effectiveness for their area, ensuring academic excellence and accreditation compliance; provides an outstanding student experience; manages faculty and staff; participates in the budget operation and program planning initiatives; promotes service, scholarship and development; and fosters an environment and work culture that elevates the chiropractic program’s reputation. To perform this job successfully, an individual should have knowledge of: Internet Software; Payroll Systems; Spreadsheet Software (Excel); Word Processing Software (Word); Electronic Mail Software (Outlook); Presentation software (PowerPoint); and classroom-specific programs like Canvas, Zoom, ExamSoft, and others.

New!

Irvine, California1 day ago

$114,950–$165,000 Per Year

This role works collaboratively with internal stakeholders and external partners, including CROs, vendors, and investigational sites, to ensure the highest quality and integrity of clinical data in support of regulatory submissions and business objectives. Overview: Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease.

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Clinical Research Jobs in Orange, CA

Jobs

Travel Nurse RN - Clinical Nurse Coordinator - $52 to $75 per hour in Newport Beach, CALancesoft Inc

Clinical Operations SpecialistA-Line Staffing Solutions LLC

Clinical Operations Specialist {169462}A-Line Staffing Solutions LLC

Medical Receptionist - Vietnamese SpeakingJobot

Office Supervisor (Medical Assistant)Jobot

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

Contracts AdminstratorKinetic Personnel Group

Shape Cardiology Excellence – Step into a Division Leadership Role TodayDepartment of Veterans Affairs

Physician | Infectious Diseases | Duarte, CACity of Hope

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

Physician| Neurologist | Irvine, CACity of Hope

Registered Nurse (RN) - Clinical Research Coordinator IIIntegrated Resources, Inc

Clinical Research CoordinatorUniversity of California, Irvine

SR. CLINICAL RESEARCH COORDINATOR - HYBRIDUniversity of California, Irvine

Clinical Research Coordinator, Full time, DaysPIH Health

Clinical Research Coordinator-RN IIIconma

Clinical Research Coordinator-RN IIApidel Technologies

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

Asst. Clinical Research Coordinator - HybridUniversity of California, Irvine

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

Clinical Research CoordinatorWake Research

Clinical Research NavigatorUniversity of California, Irvine

Clinical Research AssistantCare Access

Clinical Research Manager - HybridUniversity of California, Irvine

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

Clinical Research ManagerUniversity of California, Irvine

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

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

Clinical Research SupervisorUniversity of California, Irvine

Sr. Clinical Research RepresentativeOQSIE

ASST. RESEARCH DATA COORDINATOR - HYBRIDUniversity of California, Irvine

Research Data Coordinator - HybridUniversity of California, Irvine

APP Sub-Investigator/Clinical Trial RaterWake Research

Director, Quality (Clinical Laboratory)Quest Diagnostic

Clinical Pharmacist Specialist-IDSCity of Hope

Clinical Trial Assistant (Remote)Cordis

Field Clinical SpecialistGateway Recruiting

Clinical Operations Spec 1Lancesoft

Vice President, Research Integrity & ComplianceUniversity of California, Irvine

Movement Disorders - Health Sciences Clinical Professor or Clinical Neurology SeriesUniversity of California Irvine

Director, Clinical Education - Physician Assistant (Sign on Bonus)West Coast University, Inc.

Spec 1, Clinical OperationsTechDigital Corporation

Clinical Data CoordinatorApidel Technologies

Research Scientist - Simply BiotechTalentZok

Clinical Pharmacist - OncologyElevance Health

Clinical Specialist - California - IHFMEdwards Lifesciences

Program Director of Pre-Clinical Education, Los Angeles College of ChiropracticSouthern California University

Clinical Study ManagerCordis

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