125 study coordinator jobs at 67 companies in California
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Study Coordinator - Freelance
San Diego, California, United States
OnsiteContract, Part Time
TFS HealthScience: Global Contract Research Organization providing clinical development and resourcing services.
2+ YOE2+ years clinical research or healthcare experience; background as study coordinator/nurse or life sciences degree; knowledge of ICH-GCP and clinical trial processes; fluent English; proficient in MS Office; strong organization and communication skills.
UCLA Health: Provides comprehensive hospital services and academic medical research.
Coordinate clinical study operations from setup through closeout, ensure protocol and regulatory compliance (FDA/ICH GCP), strong communication, organization, computer and data-entry skills, and ability to meet deadlines.
Principal Research Associate/ Toxicology Study Coordinator
Carlsbad, California, United States
$111k-$142k/yrOnsiteFull Time
Ionis PharmaceuticalsNASDAQ: IONS: Discovers and develops RNA-targeted medicines for serious diseases.
8+ YOEBS/MS in life sciences,8+ years pharmaceutical/CRO toxicology study experience, GLP knowledge, study coordination, data review, strong communication and organizational skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Adobe Acrobat, JMP
Archon Business Group: Operates specialized eye care clinics and ambulatory surgery centers.
2+ YOEBachelor's preferred or 2+ years clinical research experience; HSP and GCP certification (or obtain within 5 business days); experience with clinical trial systems; strong communication and organizational skills.
City of Hope: Medical research and treatment center for cancer and diabetes.
2+ YOECoordinate oncology clinical trials including recruitment, informed consent, protocol execution, data management, and regulatory compliance. Requires bachelor’s degree (or substitute experience), minimum 2 years research/clinical experience, and various certifications within specified timeframes.
Tata Consultancy ServicesNational Stock Exchange of India: TCS: Global provider of IT services, consulting, and business solutions.
2+ YOEBS in Computer Science/HCI or related, 2+ years experience (8-10 years indicated), experience running in-person user studies, data collection, SSH/command-line troubleshooting, participant coordination, and basic data processing.
United States or Colorado or California or Illinois or New York or Washington or District of Columbia
$105k-$131k/yrRemoteFull Time
DLB Associates: Provides engineering and commissioning services for mission-critical data centers.
5+ YOEBachelor's in electrical engineering (ABET), minimum 5 years electrical engineering experience, intermediate knowledge of power system studies (short-circuit, load flow, arc flash, protection coordination, transient stability), proficiency with ETAP/PSS/E/SKM/EasyPower and Microsoft Office, ability to work remotely and travel up to 10%.
SKM Powertools, EasyPower, ETAP, PSS/E, Microsoft Excel, Microsoft Word, Microsoft Outlook, Microsoft PowerPoint, Microsoft Teams
Federal Work Study Student Position - Technical Support Coordinator
San Diego or New Mexico or Florida or Massachusetts
$26/hrRemotePart Time
California Institute of Applied Technology: A private technical college providing IT degrees and certifications.
Must be a CIAT student eligible for Federal Work Study, in good academic standing (min GPA 2.0, 3.0+ preferred), strong communication and problem-solving, able to work up to 20 hours/week and reside in California for remote work.
UCSF Health: Academic medical center providing advanced patient care and research.
Support and coordinate clinical cardiology studies, manage study data and regulatory documents, communicate with stakeholders, ensure compliance with research regulations; willingness for limited travel.
Committee on Human Research (CHR) iMEDris, EPIC, Electronic Medical Records (EMR), Access, Stata, SASS, SPSS, Teleform
University of California, San Francisco: Public research university dedicated to health sciences and education.
Coordinate clinical research studies, recruit and enroll subjects, collect and manage data, maintain regulatory compliance, and communicate with patients and investigators.
Microsoft Word, Microsoft Excel, Access, Stata, SASS, SPSS, Teleform, Committee of Human Research (CHR) online iMEDris system, Electronic Medical Records (EMR)
Alliance Clinical Network: Operates medical research sites for Phase I-IV clinical trials.
Support coordination and execution of clinical research studies, participant screening, consent, data collection, specimen handling, and regulatory compliance; knowledge of GCP/HIPAA preferred.
Electronic data capture systems, Clinical trial management software, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
Parker-Anderson Enrichment: Site Coordinator, Study Skills in La Mirada
Norwalk, California, United States
$18-$25/hrOnsitePart Time
Parker-Anderson Enrichment: Provides after-school enrichment and STEAM programs for K-8 students.
Proven after-school or educational leadership, available Mon–Fri 2–6 PM, able to supervise students and instructors, manage sign-in/snack procedures, and communicate with parents and school staff.
Stanford University: A private research university providing higher education and research.
2+ YOECoordinate clinical studies, obtain consent, collect specimens and data, maintain regulatory documentation, and ensure protocol compliance; requires 2 years related experience or a bachelor's degree.
Stanford University: Private research university providing academic education and medical services.
2+ YOEAssociate's degree + 2 years related experience or Bachelor's in a related field; experience coordinating clinical studies, participant consent, specimen collection, regulatory compliance, Microsoft Office proficiency, strong interpersonal skills.
Helios Clinical Research: Integrated clinical trial site network for medical research
2+ YOEBachelor's preferred, 2 years clinical research experience, regulatory and study coordination skills, phlebotomy, vital signs and ECG competence, participant recruitment and informed consent.
Clinical Research Coordinator I - Westside Los Angeles
Los Angeles, California, United States
$27/hrOnsiteFull Time
Irvine Clinical Research: Conducts clinical trials specializing in neurology and psychiatry.
Coordinate clinical trial operations, perform study procedures per GCP/protocols, maintain study data, recruit and screen participants; bachelor's/masters/nursing degree required; strong attention to detail and English proficiency.
Cedars-Sinai: Provides academic medical care, specialized treatment, and biomedical research.
1+ YOECoordinate clinical studies, screen and consent patients, maintain source documents and CRFs, ensure timely data entry and regulatory compliance; 1+ year clinical research experience, HS diploma minimum, bachelor\u0002s preferred.
Troy or California or Massachusetts or New York or Colorado or Hawaii or Illinois or Maryland or Minnesota or New Jersey or Vermont or Washington or District of Columbia
$78k-$155k/yrOnsiteFull Time
Lockheed MartinNYSE: LMT: Designs and manufactures global security and aerospace systems.
5+ YOEBachelor's degree or equivalent experience with 5+ years (or 4+ with related Master's); familiarity with Lean Six Sigma, analytical tools, workflow studies, project management, databases and data analytics; strong communication and organizational skills.
Lean Six Sigma, SAP, Solumina, JIRA, Tableau Dashboards