2,415 Results for

Clinical Research Jobs in California

Jobs

Dermatologist - Clinical Educator UCLA Health - Division of Dermatology

Santa Barbara, CA

Our locations include Downtown LA, West LA, San Luis Obispo, Santa Barbara, Ventura, Calabasas, Westwood, Santa Monica, Burbank, Century City, Encino, Pasadena, Redondo Beach, Santa Clarita, Thousand Oaks and Torrance. The Division of Dermatology in the Department of Medicine at the David Geffen School of Medicine at UCLA is seeking applicants for full-time clinician educators in the Health Sciences Clinical Professor series at the Instructor, Assistant, Associate and full Professor ranks in an academic setting across our network of campus and community practices for medical dermatology.

2 days ago

Clinical Supervisor, BCBA Accel Therapies

Chino, CA

$90,000–$95,000 / year

As a Clinical Supervisor, you’ll join an organization that prioritizes your growth and impact by reducing administrative burdens and allowing you to focus on what matters most — delivering high-quality clinical care. Our service model may vary by location, but across all sites, you’ll be supported by a team structure that promotes collaboration, development, and strong clinical outcomes.

3 days ago

Clinical Director, BCBA Accel Therapies

Lake Arrowhead, CA

$100,000–$110,000 / year

Accel Therapies is seeking experienced and mission-driven Clinical Directors (BCBAs) to lead our center-based teams. As a Clinical Director, you’ll mentor Clinical Supervisors, guide program integrity, and help drive high-quality outcomes for the families we serve.

3 days ago

Local Contract Social Work - Licensed Clinical Social Worker - $60 per hour VeeAR Health

Fairfield, CA

Job Description: Duties: Provides direct clinical social work service, counseling, discharge planning, and case management services to hospital patients and their families including assessment and documentation of emotional, social, financial, environmental or follow-up referral needs. Ability to build and maintain constructive relationships with team members, external service providers, System managers, and department staff – often within the context of competing interests – essential.

2 days ago

Cardio-Oncology & Heart Failure Cardiologist – Palo Alto, CA | Advanced Imaging & Research Program | Shareholder Track Palo Alto Foundation Medical Group

Palo Alto, CA

Our current program has significant support with a dedicated program manager, experienced NPs, philanthropic funding, and Sutter Administration, with future goals of developing a robust data infrastructure for ongoing research endeavors including reduction of readmissions and telemedicine management. Candidate should have specific training in cardio-oncology (or at least 2 years of clinical work), ideally with leadership experience to further develop our current cardio-oncology program, and expertise in managing systolic and diastolic heart failure of various etiologies.

Today

Clinical + Metabolic Geneticist Loma Linda University Faculty Medical Group

Colton, CA

The Children's Hospital is one of the few centers for pediatric cardiac transplants and ECMO in California and is developing a Perinatal Care Center with a focus on prenatal diagnosis to better serve the large population of high-risk pregnancies and infants with prenatally diagnosed congenital anomalies. The diversity of the clinical genetics practice is extraordinary, offering both depth and breadth of experience in all areas including neurogenetics, cardiogenetics, cancer genetics, dysmorphology, and congenital anomalies.

2 days ago

Transplant/Cell Therapy & Malignant Hematology - Physician Scientist Loma Linda University Faculty Medical Group

San Bernardino, CA

Qualification requirements include MD (or foreign equivalent), completion of fellowships in Medical Oncology and/or Hematology, TCT fellowship (or equivalent experience) preferred, and Internal Medicine, Hematology, or Medical Oncology board eligible or certified; or completion of fellowships in Pediatric Hematology/Oncology or Immunology, TCT fellowship (or equivalent experience), and Pediatrics, Pediatric Hematology/Oncology, or Immunology board eligible or certified. Successful candidates will have a primarily research laboratory assignment with dedicated laboratory space and a generous start up package, but will also be expected to develop, conduct, and participate in translating laboratory research into clinical applications, other collaborative research in blood and marrow transplantation, and cellular immunotherapy.

2 days ago

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

San Francisco, California

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. Qualifications: Must have a minimum of a Bachelor’s degree in a health or science related field; Experience as a Clinical Research Coordinator (minimum 1 year); 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.

14 days ago

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

Los Angeles

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.

14 days ago

Senior Clinical Research Associate - Oncology Zp Group Llc

San Francisco, CA

$120,000–$145,000 / year

Keywords: Senior Clinical Research Associate, Senior CRA, Clinical Research Associate, Oncology Clinical Trials, Oncology Research, Phase II Clinical Trials, Phase III Clinical Trials, Clinical Monitoring, Independent Monitoring, Site Monitoring, Site Management, Clinical Operations, ICH-GCP, FDA Regulations, GCP Compliance, Clinical Trial Management, Source Data Verification, SDV, Source Data Review, SDR, CRF Review, Case Report Forms, Site Initiation Visits, SIV, Interim Monitoring Visits, IMV, Closeout Visits, COV, Investigative Sites, Study Start-Up, Patient Enrollment, Site Performance, Risk Management, Protocol Compliance, Clinical Development, Biotechnology, Biotech Sponsor, Pharmaceutical Research, CRO, Sponsor-Facing, Trial Execution, Site Oversight, Data Quality, Inspection Readiness, Regulatory Compliance, Oncology Studies, Clinical Research, Clinical Trial Oversight, Clinical Monitoring Visits, Site Relationships, Clinical Study Management. Responsibilities for the Senior Clinical Research Associate include: Independently monitoring Phase II-III Oncology clinical trials to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.

6 days ago

Clinical Research Associate / Senior Clinical Research Associate CareTechPros

San Francisco, California

We are looking for a Clinical Research Associate to manage clinical trial activities from initiation to closeout. The ideal candidate is organized, detail-oriented, and experienced in managing complex clinical trials.

23 days ago

Sr Clinical Research Coordinator Clinical Research Network Office UCSF Medical Center

Berkeley, CA

Positions at Sr CRC level may perform expert and efficient integration of multiple complex programmatic activities, applying a sophisticated medical knowledge base, substantial leadership skills, and effectively working with a variety of internal (clinicians, investigators, clinical staff, administration, Institutional Review Board (IRB), human resources, contracts and grants) and external (industry sponsors, coordinating centers, FDA, NIH) stakeholders, exhibiting an in-depth knowledge of specific programs. The Sr CRC will perform independently or with general direction at the fully operational level of the series to execute, manage, coordinate research protocols, and train staff, as directed by the Principal Investigator (PI), Program Director, and Clinical Research Manager (CRM).The incumbent may have central responsibility for assisting with IRB approval and compliance, ensuring subject recruitment and adequate enrollment, executing research procedures, and developing site and study specific workflows.

8 days ago

Senior Clinical Research Associate - Remote Position Puma Biotechnology Inc

Los Angeles, CA

Remote

$140,000–$165,000 / year

Conducts all activities involved in on-site visits consistent with the applicable Clinical Monitoring Plan (CMP), SOPs, and ICH GCP for site qualification, site initiation, interim monitoring, site close-out, and other site visits (eg, booster visits). The physical demands of the home office are normally associated with extended amounts of time sitting and using office equipment (including a computer, keyboard, and mouse), standing, walking, sitting, speaking, and hearing.

30+ days ago

Senior Clinical Research Associate - Oncology - West Coast - FSP Parexel International Corp

Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks. Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics.

30+ days ago

Clinical Research Associate I - Butte Lab - Department of Neurosurgery (Per Diem) Cedars-Sinai Medical Center

Los Angeles, CA

The job will provide an outstanding opportunity to work with a multidisciplinary team involving optical engineers, mechanical engineers, electrical engineers, biomedical engineers as well as surgeons, pathologists, and other medical personnel. The Butte Lab is developing novel intra-operative imaging/visualization technologies to aid surgeons in achieving near-complete tumor excision.

30+ days ago

Clinical Research Associate II/Sr. CRA- CA/AZ IRE

California

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

18 days ago

Senior Clinical Research Associate - CNS/Rare Disease - West Coast Worldwide Clinical Trials Holdings Inc

$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.

25 days ago

Senior Clinical Research Associate Protagonist Therapeutics Inc

Newark, CA

$135,000–$150,000 / year

Support study vendor management by performing key activities as delegated by study CTM, including but not limited to: Participate in evaluation of new vendors (CROs, labs, central readers, EDC, etc.) by drafting and/or reviewing RFPs, analyzing responses and drafting work orders for select vendors • Manage the day to day interactions with select study vendor(s), such as a central or specialty lab including developing training materials, lab manuals and acting as first point of contact for issue and query escalation and resolution. Part of the clinical study team and takes a lead on execution by performing key activities as delegated by the Clinical Study lead, including but not limited to: Develop and/or review key study operational documents (e.g., study reference manual, laboratory and pharmacy manuals, data management plan, query generation, monitoring plan; review site audit reports) •.

30+ days ago

Experienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas Available Thermo Fisher Scientific

San Diego, California

At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.

4 days ago

Sr. Clinical Research Associate Dendreon Corporation

Seal Beach, California

Systems Proficiency: Proficiency with clinical research systems, including Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), Microsoft Office applications (Excel, Word, PowerPoint, etc), Smartsheets. Responsibilities: Site Monitoring & Management: Conduct remote and on-site visits (site assessment, initiation, routine monitoring, and close-out); Familiar with Risk Based Monitoring (RBM), verify source data, ensure ongoing subject safety review, and audit IP accountability per the monitoring plan.

25 days ago

Clinical Research Associate Alto Neuroscience Inc

Remote

$75,000–$120,000 / year

PRIMARY ROLE The Clinical Research Associate (CRA) is responsible for the oversight of assigned investigative sites in accordance with all applicable protocols, project plans, Sponsor SOPs, GCP guidelines, and regulatory requirements from site initiation through site close out. The CRA assists the Clinical Trial Manager and/or Clinical Project Manager by managing their assigned clinical sites to ensure enrollment, timely review of data, identification of site issues, and prompt resolution of issues.

30+ days ago

Senior Clinical Research Associate Epicrispr Biotechnologies Inc

South San Francisco, CA

$115,000–$121,000 / year

Support clinical trial manager with site management, including: site startup activities, co-monitoring visits alongside CRO, reviewing monitoring visit reports, coordinating vendor trainings, reviewing study newsletters, and other duties as needed, in alignment with study priorities and CTM guidance. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.

30+ days ago

Clinical Research Associate - Irvine, CA MDxHealth SA

Irvine, CA

$64,500–$75,000 / year

The CRA will monitor specimen TAT, set up new study accounts, manage current study accounts, requests, and track specimens, and ensure that all study specimens are adhering to the SOP. The CRA will monitor clinical study data for completeness and accuracy, perform data cleaning, reconciliation of data queries and generate data reports as needed.

30+ days ago

Clinical Research Associate Veracyte Inc

South San Francisco, CA

$110,000–$127,000 / year

Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. Based at the San Francisco campus, the CRA partners with Clinical Affairs, R&D, Medical Affairs, and Laboratory Operations to ensure high-quality, compliant, and timely study execution.

30+ days ago

Clinical Research, Associate I Abbott Laboratories

Alameda, CA

$73,900–$116,000 / year

General Medical Devices: Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ngersticks. Demonstrate excellence in teamwork, solid interpersonal and communication skills including building rapport with team members/peers, study site staff, and clinical management.

6 days ago

Clinical Research Associate I Evotec SE

South San Francisco, CA

Remote

$90,000–$110,000 / year

The base salary range for this position at commencement of employment is expected to be $90,000 - $110,000; Base salary offered may vary depending on individual's skills, experience and competitive market value. Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.

2 days ago

Clinical Research, Associate I Abbott

Alameda, California

General Medical Devices: Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ngersticks. Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday) .

7 days ago

Senior Clinical Research Associate IRE

Los Angeles, California

Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.

10 days ago

Clinical Research Associate IRE

Long Beach, California

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

10 days ago

Clinical Research Associate Contractor Freenome Inc

Remote

You are passionate about clinical research, attention to detail and Good Clinical Practice, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. Write and submit reports of investigational site findings and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate.

30+ days ago

Clinical Research Nurse-Lymphoma City of Hope

Duarte, CA

City of Hope's 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. Join our team as a Clinical Research Nurse, where you'll play a vital role in guiding patients through innovative clinical trials while collaborating with a multidisciplinary team of physicians, Clinical Research Associates (CRA), pharmacists, and coordinators.

30+ days ago

Senior Oncology Clinical Research Associate Zp Group Llc

Los Angeles, CA

$145,000–$175,000 / year

The Senior Contract Oncology Clinical Research Associate (SCRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Senior Contract Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study.

30+ days ago

Senior Clinical Research Associate Crinetics Pharmaceuticals Inc

$119,000–$149,000 / year

Train and assist site coordinators, investigators, and CRO (as applicable) in collecting data and executing the study in a timely manner that meets the protocol requirements and timelines/milestones; serve as a resource to site coordinators, investigators and other staff members regarding investigational products and protocols. Conduct site visits including but not limited to qualification visits, initiation visits, interim monitoring visits, and close-out visits; generate clear, comprehensive, and accurate visit reports and letters in a timely manner.

30+ days ago

Clinical Research Associate II Corcept Therapeutics Inc

Redwood City, CA

$129,400–$152,300 / year

With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. The pay range that the Company reasonably expects to pay for this headquarters-based position is $129,400 - $152,300; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

30+ days ago

Sr. Clinical Research Associate Structure Therapeutics Inc

South San Francisco, CA

$135,000–$150,000 / year

Overall management of selected clinical sites including acting as a point of escalation and oversight of CRO monitoring activities, which includes monitoring visit report review, contract and budget negotiations with clinical sites. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs.

30+ days ago

Senior Clinical Research Associate Rakuten Medical Inc

San Diego, CA

Our first clinical product received marketing approval in Japan from the Ministry of Health, Labour and Welfare for ASP-1929 PIT to treat unresectable locally advanced or recurrent head and neck cancer - and is also in Phase III pivotal clinical testing globally to treat terminal cancer patients. The ideal candidate will have experience in clinical trial operation (including site monitoring, CRO/Vendor management) with previous experience with oncology (head and neck cancer preferred), combination drug-device studies preferred.

30+ days ago

Clinical Research Nurse- Transplant City of Hope

Duarte, CA

City of Hope's 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. Assess and document signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB protocol assuring that the documentation is complete and accurate in order to avoid protocol deviations.

30+ days ago

Clinical Research Coordinator II - The Angeles Clinic & Research Institute Cedars-Sinai Medical Center

Los Angeles, CA

Establishes and completes 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. The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians.

30+ days ago

Clinical Research Associate II Abbott Laboratories

Alameda, CA

$81,500–$141,300 / year

Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. General Medical Devices: Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ngersticks.

9 days ago

Clinical Research Associate II Abbott

Alameda, California

10 days ago

Senior Clinical Research Associate ICON Plc

Los Angeles, CA

$110,520–$138,150 / year

30+ days ago

Clinical Research Associate II ICON Plc

$91,336–$114,170 / year

28 days ago

Clinical Research Associate ICON Plc

Long Beach, CA

$91,336–$114,170 / year

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

9 days ago

Clinical Research Associate, Sponsor Dedicated, IQVIA IQVIA Holdings Inc

Carlsbad, CA

$71,900–$182,000 / year

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

30+ days ago

Sr Clinical Research Associate - Oncology United BioSource LLC

Remote

Brief Description: Monitors clinical trials and observational studies ensuring protocol adherence, managing site activities, and overseeing data collection and integrity. Enters site visits, site monitoring reports, follow-up letter sent date and site contacts into UBC's Clinical Trial Management System (CTMS).

14 days ago

Sr. Clinical Research Associate (Field) Shifamed

Los Gatos, California

Remote

Supira Medical, a clinical-stage Shifamed Portfolio Company, is developing a low-profile, high continuous flow percutaneous ventricular assist device (pVAD) to provide temporary mechanical circulatory support in high risk percutaneous coronary interventional (HRPCI) procedures as well as patients suffering from cardiogenic shock. ABOUT SHIFAMED Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.

23 days ago

Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources Rady Children's Hospital

San Diego, CA

$34.14–$46.94 / hour

Responsibilities may include but are not limited to: submission of protocols & renewals to IRB & scientific review boards; management & submission of electronic data forms to Sponsors, CROs & regulatory agencies; screening for eligibility; monitoring and timely reporting of adverse events; toxicities and protocol deviations; scheduling subjects' visits; coordinating clinical, laboratory and data management activities; processing and submitting laboratory specimens. Assist with initiation, implementation and management of research projects in accordance with GCP, FDA, HIPAA & all required regulatory guidelines, with an emphasis on pediatric clinical research studies.

21 days ago

Clinical Research Coordinator Associate (12-Month Fixed-Term) Stanford University

Stanford, CA

$34.56–$40.30 / hour

The Department of Medicine (DoM) Clinical Research Hub (CRH) at Stanford University is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies in the disciplines of Nephrology, Hospital Medicine and other therapeutic areas. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location, and external market pay for comparable jobs.

17 days ago

Senior Clinical Research Coordinator UCSF Medical Center

San Francisco, CA

It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository. Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies, and continually adjusting strategies to meet current recruitment goals.

30+ days ago

Clinical Research Associate II Imperative Care

Campbell, CA

Full time

The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Provide in-house clinical operations support by assisting with study documentation, site coordination, and day-to-day clinical trial activities to help ensure successful study execution.

30+ days ago

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Clinical Research Jobs in California

Dermatologist - Clinical Educator UCLA Health - Division of Dermatology

Clinical Supervisor, BCBA Accel Therapies

Clinical Director, BCBA Accel Therapies

Local Contract Social Work - Licensed Clinical Social Worker - $60 per hour VeeAR Health

Cardio-Oncology & Heart Failure Cardiologist – Palo Alto, CA | Advanced Imaging & Research Program | Shareholder Track Palo Alto Foundation Medical Group

Clinical + Metabolic Geneticist Loma Linda University Faculty Medical Group

Transplant/Cell Therapy & Malignant Hematology - Physician Scientist Loma Linda University Faculty Medical Group

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

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

Senior Clinical Research Associate - Oncology Zp Group Llc

Clinical Research Associate / Senior Clinical Research Associate CareTechPros

Sr Clinical Research Coordinator Clinical Research Network Office UCSF Medical Center

Senior Clinical Research Associate - Remote Position Puma Biotechnology Inc

Senior Clinical Research Associate - Oncology - West Coast - FSP Parexel International Corp

Clinical Research Associate I - Butte Lab - Department of Neurosurgery (Per Diem) Cedars-Sinai Medical Center

Clinical Research Associate II/Sr. CRA- CA/AZ IRE

Senior Clinical Research Associate - CNS/Rare Disease - West Coast Worldwide Clinical Trials Holdings Inc

Senior Clinical Research Associate Protagonist Therapeutics Inc

Experienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas Available Thermo Fisher Scientific

Sr. Clinical Research Associate Dendreon Corporation

Clinical Research Associate Alto Neuroscience Inc

Senior Clinical Research Associate Epicrispr Biotechnologies Inc

Clinical Research Associate - Irvine, CA MDxHealth SA

Clinical Research Associate Veracyte Inc

Clinical Research, Associate I Abbott Laboratories

Clinical Research Associate I Evotec SE

Clinical Research, Associate I Abbott

Senior Clinical Research Associate IRE

Clinical Research Associate IRE

Clinical Research Associate Contractor Freenome Inc

Clinical Research Nurse-Lymphoma City of Hope

Senior Oncology Clinical Research Associate Zp Group Llc

Senior Clinical Research Associate Crinetics Pharmaceuticals Inc

Clinical Research Associate II Corcept Therapeutics Inc

Sr. Clinical Research Associate Structure Therapeutics Inc

Senior Clinical Research Associate Rakuten Medical Inc

Clinical Research Nurse- Transplant City of Hope

Clinical Research Coordinator II - The Angeles Clinic & Research Institute Cedars-Sinai Medical Center

Clinical Research Associate II Abbott Laboratories

Clinical Research Associate II Abbott

Senior Clinical Research Associate ICON Plc

Clinical Research Associate II ICON Plc

Clinical Research Associate ICON Plc

Clinical Research Associate, Sponsor Dedicated, IQVIA IQVIA Holdings Inc

Sr Clinical Research Associate - Oncology United BioSource LLC

Sr. Clinical Research Associate (Field) Shifamed

Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources Rady Children's Hospital

Clinical Research Coordinator Associate (12-Month Fixed-Term) Stanford University

Senior Clinical Research Coordinator UCSF Medical Center

Clinical Research Associate II Imperative Care

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