597 Results for

Clinical Research Manager Jobs in Irvine, CA

Jobs

Costa Mesa, CA

Required Certifications & Licensure: -Registered Nurse in the State of California - Current and in good standing. -Minimum of Five (5) years' experience in nursing and Three (3) years' of experience in area of specialty.

1 day ago

Huntington Beach, California

As a Clinical Research Manager, you will own end-to-end US IDE study operations, leading a team of clinical research professionals, ensuring regulatory compliance across all active sites, and driving the clinical strategy that will help bring the world’s first Total Artificial Heart to patients who need it most.

Collaborate on clinical strategy and author key clinical documents including clinical study protocols, clinical study reports, clinical evaluation plans/reports, annual progress reports, risk-benefit analyses, and clinical marketing materials.

30+ days ago

Orange, California

p style="margin:0px">*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. Please utilize the links listed here to learn more about our compensation practices and benefits.

30+ days ago

Riverside, CA
$100,000–$105,000 / year
The Site Manager owns meeting or exceeding financial targets, KPIs, and patient enrollment, as well as champions screening, patient retention, and partnering with other Headlands centralized departments or sites.
Partners with Human Resources and Management when hiring new employees for the site by reviewing candidate credentials, conducting interviews, and giving input about potential new hires.
21 days ago

Irvine, CA
2025 University of California, Irvine, UCI Health, and UC Regents. Sign-up to be notified of hiring events, newly posted job opportunities, and much more.
30+ days ago

Irvine, CA
p>2025 University of California, Irvine, UCI Health, and UC Regents.
Sign-up to be notified of hiring events, newly posted job opportunities, and much more.
30+ days ago

Riverside, California
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Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.

15 days ago

New
Irvine, CA
You will provide leadership to the organization to develop research programmatic infrastructure, operational workflows and approval processes, direct institutional use of the Research Core services or research study, financial, or research administration resources.
This position works closely with Cherng Center Research Director, leaders and staff to support and advance the mission of the Center, has a high level of autonomy, collaborates with contributors across the organization (research, administrative, medical, and support personnel), and is a key position in the Program.
2 days ago

Riverside, California
p>Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
11 days ago

Riverside, CA
$29–$33 / hour
Part time
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
11 days ago

CA
Remote
$97,000–$193,000 / year
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
16 days ago

Orange, California
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.

11 days ago

Anaheim, California
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Collects, 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.
30+ days ago

Riverside, California
Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
8 days ago

Los Alamitos, California
Once training is completed, you will be scheduled for your normal shift going forward.

Hourly Range: $32.00 - $34.00/hour (Depending on education, experience, and skillset)

Job Summary: .
Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
11 days ago

Riverside, California
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Hourly Range: $29.00 - $30.00/hour + 4hrs of OT each day (Depending on education, experience, and skillset)

Job Summary: .
Working Shift: 3 X 12 Shifts: 6:00 pm - 6:00 am + Availably to work weekends as part of your normal schedule
Paid training is for 2 weeks, working a morning shift.

8 days ago

Anaheim, California
Assist the Regulatory Specialists/Manager in maintaining clinical trial documents for submission to regulatory agencies in accordance to site SOPs, ICH, GCP, and FDA guidelines. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
10 days ago

Riverside, CA
$29–$30 / hour
Part time
Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
8 days ago

Anaheim, CA
$20–$21.50 / hour
Part time
Assist the Regulatory Specialists/Manager in maintaining clinical trial documents for submission to regulatory agencies in accordance to site SOPs, ICH, GCP, and FDA guidelines. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
10 days ago

Anaheim, CA
$30–$35 / hour
Part time
Collects, 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.
30+ days ago

Riverside, CA
$32–$34 / hour
Part time
Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Working Shift: 3 X 12 Shifts: 6:00 pm - 6:00 am + Availably to work weekends as part of your normal schedulePaid training is for 2 weeks, working a morning shift.
8 days ago

Los Alamitos, California
Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
9 days ago

Los Alamitos, California
We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability.
21 days ago

Anaheim, California
p>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.
28 days ago

Bellflower, California
li>Develops budget and ensures financial and operational metrics are meeting organizational objectives by identifying, analyzing, and monitoring issues that affect profitability, growth, and productivity. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
30+ days ago

Anaheim, CA
$20–$21 / hour
Part time
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.
28 days ago

Los Alamitos, CA
$32–$34 / hour
Part time
Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
9 days ago

Riverside, CA
$20–$22.50 / hour
Part time
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.
11 days ago

Bellflower, CA
Part time
Preparing 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.
30+ days ago

Bellflower, California
li>Preparing 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.
30+ days ago

Los Alamitos, California
Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
8 days ago

Bellflower, CA
$130,000–$150,000 / year
Part time
Develops budget and ensures financial and operational metrics are meeting organizational objectives by identifying, analyzing, and monitoring issues that affect profitability, growth, and productivity. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
30+ days ago

Los Alamitos, CA
$20–$21.50 / hour
Part time
We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability.
21 days ago

Irvine, CA
$80,000–$95,000 / year
Partner with Territory Managers to achieve sales quotas in all Alternate Care markets; Identify problem areas to implementation of Masimo technology and work to resolve these issues; Work with Territory Managers to coordinate Alternate Care customer installations in conversion to Masimo SET, Rainbow, SpHb and PSN; Manage or assist with the installation process and personnel; Coordinate clinical evaluations of Masimo technology for both clinical investigators, customers, and OEM partners; Support Trade Shows; Assist in the clinical education, follow up, and training needs of clinicians and sales force; Participate in continued evaluation of new products and assist in beta testing; Perform clinical evaluation of Masimo technology including customer research and focus groups, as required; Extensive domestic travel is a major job component; Performs other duties or special projects as requested; Minimum & Preferred Qualifications and Experience: Minimum Qualifications. Five or more years of experience in the clinical arena related to alternate care markets; Very strong, written, verbal communication and interpersonal skills; Must be results oriented with positive "can do" attitude with a sense of urgency to get things done; Comfortable in high visibility situations, exhibits strong self-confidence; Proven track record in persuading clinicians to consider and embrace new ideas, with an emphasis on new patient care processes based on clinical evidence and new, innovative technologies; Independent problem solver; Organized and detail oriented with a demonstrated ability to manage multiple projects simultaneously; Must be able to professionally communicate effectively with management, executives, physicians, staff, peers, sales reps and customers; Must be able to maintain an extensive domestic travel schedule; Preferred Qualifications.
30+ days ago

Los Alamitos, CA
$20–$21 / hour
Part time
Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
8 days ago

Los Alamitos, CA
$20–$22.50 / hour
Part time
Preparing 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.
14 days ago

Irvine, California
p style="margin:0px">*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. Please utilize the links listed here to learn more about our compensation practices and benefits.

17 days ago

Harbor City, CA
$67,800–$87,670 / year
For-jobs-where-work-will-be-performed-in-unincorporated-LA-County,-the-employer-provides-the-following-statement-in-accordance-with-the-Los-Angeles-County-Fair-Chance-Ordinance.-Criminal-history-may-have-a-direct,-adverse,-and-negative-relationship-on-the-following-job-duties,-potentially-resulting-in-the-withdrawal-of-the-conditional-offer-of-employment: Consistently-supports-compliance-and-the-Principles-of-Responsibility-(Kaiser-Permanente's-Code-of-Conduct)-by-maintaining-the-privacy-and-confidentiality-of-information,-protecting-the-assets-of-the-organization,-acting-with-ethics-and-integrity,-reporting-non-compliance,-and-adhering-to-applicable-federal,-state,-and-local-laws-and-regulations,-accreditation,-and-licensure-requirements-(where-applicable),-and-Kaiser-Permanente's-policies-and-procedures. Criminal history may have a direct, adverse, and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: Consistently supports compliance and the Principles of Responsibility (Kaiser Permanente's Code of Conduct) by maintaining the privacy and confidentiality of information, protecting the assets of the organization, acting with ethics and integrity, reporting non-compliance, and adhering to applicable federal, state, and local laws and regulations, accreditation, and licensure requirements (where applicable), and Kaiser Permanente's policies and procedures.
30+ days ago

Orange, CA
Under 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.
30+ days ago

Fountain Valley, CA
$28–$35 / hour
Conduct patient visits and ensure adherence to study protocols, collecting and processing biological specimens (blood/urine) and performing procedures such as ECGs and vital signs monitoring. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
22 days ago

Fountain Valley, CA
$28–$35 / hour
li>Conduct patient visits and ensure adherence to study protocols, collecting and processing biological specimens (blood/urine) and performing procedures such as ECGs and vital signs monitoring.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
30+ days ago

Los Angeles, CA
$26.77–$34.32 / hour
When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational consideration.
Interacts closely with quality assurance teams to ensure data accuracy on Clinical Research Forms (eCRFs/CRFs) prior to submission for in-house, National Cancer Institute (NCI) sponsored and Cooperative Group studies.
30+ days ago

Ontario, CA
p>• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
30+ days ago

Irvine, CA
City of Hopes growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago, and Phoenix. As a manager, you will assist the Executive Director, Clinical Research, Care Coordination (ED, CRCC) in the responsibilities for the daily operational needs of the Clinical Research Nurses (CRNs) in the Clinical Trials Office (CTO) in Orange County.
30+ days ago

Irvine, CA
p>The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
30+ days ago

Irvine, California
Remote
li>Where appropriate, responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits and appropriate documentation (confirmation, follow-up letters, communication logs, as required). For more details regarding Tarsus benefits, please visit: https://eb.alliant.com/26tarsusbenefitssnapshot.
15 days ago

Anaheim, CA
Remote
$170,000–$210,000 / year
p>Responsible for representing Sobis products and services to a defined customer base, generating and growing sales and consistently achieving or exceeding sales goals within a specific geographic area and actively promotes the appropriate use of Sobi products to healthcare professionals in accordance with all Corporate, PhRMA, and OIG guidelines. As a sales leader, the CAM is expected to achieve territory sales by executing Plan of Action (POA) marketing strategies, which includes delivering branded sales messages to customers, representing Sobi at local meetings, and achieving or exceeding sales targets.
30+ days ago

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Clinical Research Manager Jobs in Irvine, CA

CLINICAL NURSE NAVIGATOR I - 6 TalentBurst, Inc.

Clinical Research Manager BiVACOR

Clinical Research Manager University of California, Irvine

Clinical Research Site Manager Headlands Research Inc

Clinical Research Manager - Hybrid University of California

Clinical Research Manager University of California

Clinical Research Site Manager Headlands Research

Administrative Clinical Research Programs Manager - Cherng Family Center for Integrative Oncology City of Hope

Clinical Research Coordinator - Clinical Research CenExel

Clinical Research Coordinator - Clinical Research Clinical Innovation Inc.

Senior Clinical Research Associate - CNS/Psychiatry - West Coast - Remote Worldwide Clinical Trials Holdings Inc

Asst. Clinical Research Coordinator - Hybrid University of California, Irvine

Clinical Research Coordinator - Hybrid University of California, Irvine

Clinical Research - Regulatory Specialist CenExel

Licensed Vocational Nurse - Clinical Research (Part-Time Weekends) CenExel

Licensed Vocational Nurse - Clinical Research (Friday, Saturday, Sunday) CenExel

Licensed Vocational Nurse - Clinical Research (6:00 pm - 6:00 am) CenExel

Regulatory Assistant - (Clinical Research) CenExel

Licensed Vocational Nurse - Clinical Research (Part-Time Weekends) Clinical Innovation Inc.

Regulatory Assistant - (Clinical Research) Anaheim Clinical Trials, LLC

Clinical Research - Regulatory Specialist Anaheim Clinical Trials, LLC

Licensed Vocational Nurse - Clinical Research (6:00 pm - 6:00 am) Clinical Innovation Inc.

Licensed Vocational Nurse - Clinical Research (11:00 pm - 7:30 am) CenExel

Phlebotomist (Clinical Research) CenExel

Medical Assistant - Clinical Research CenExel

Director of Clinical Research Site Operations CenExel

Medical Assistant - Clinical Research Anaheim Clinical Trials, LLC

Licensed Vocational Nurse - Clinical Research (11:00 pm - 7:30 am) Collaborative Neuroscience Research, LLC

Medical Assistant - Clinical Research Clinical Innovation Inc.

Medical Assistant - Clinical Research (6:00 am - 6:00 pm) Clinical Innovation Inc.

Medical Assistant - Clinical Research (6:00 am - 6:00 pm) CenExel

Dietary Aide - Clinical Research CenExel

Director of Clinical Research Site Operations Collaborative Neuroscience Research, LLC

Phlebotomist (Clinical Research) Collaborative Neuroscience Research, LLC

Area Clinical Resource Manager Masimo Corp

SR. CLINICAL RESEARCH COORDINATOR - HYBRID University of California, Irvine

Dietary Aide - Clinical Research Collaborative Neuroscience Research, LLC

Medical Assistant - Clinical Research Collaborative Neuroscience Research, LLC

Licensed Vocational Nurse - Clinical Research (Friday, Saturday, Sunday) Collaborative Neuroscience Research, LLC

Asst. Clinical Research Finance Analyst University of California, Irvine

Research Associate II, Oncology Clinical Trials Kaiser Permanente

Clinical Research Assistant Pacific Neuropsychiatric Specialists Inc

Clinical Research Coordinator - Bilingual Actalent Inc

Clinical Research Coordinator Actalent Inc

Clinical Research Data Specialist I University of Southern California

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Mgr, Research Nursing Ops - OC City of Hope

Sr. Clinical Research Director (CRDN) Medtronic Plc

Sr Clinical Research Associate (CRA) the Tarsanet Internal Career Center

Hematology Clinical Account Manager/ Sr. Clinical Account Manager (Anaheim) Swedish Orphan Biovitrum AB

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