San Francisco • 50 milesRemote · Hybrid · Onsite · Field · All Environments
San Francisco • 50 milesRemote · Hybrid · Onsite · Field · All Environments
San Francisco • 50 milesRemote · Hybrid · Onsite · Field · All Environments
San Francisco • 50 milesRemote · Hybrid · Onsite · Field · All Environments
57 irb jobs at 14 companies in San Francisco, CA
1mo
Save
Mark Applied
Hide
CLIN RSCH CRD
San Francisco, California, United States
HybridFull Time
HS diploma and relevant experience; strong attention to detail, communication, multitasking, regulatory compliance, IRB/CHR familiarity and data management skills.
Committee of Human Research (CHR), iMEDris, Microsoft Excel, Microsoft Access, Stata, SASS/ SPSS, REDCap, Teleform, Microsoft Word, Electronic Medical Records (EMR)
1mo
Save
Mark Applied
Hide
Regulatory Affairs Associate
San Francisco, California, United States
$38/hr OnsiteFull Time
Coordinate and manage IRB submissions, maintain study documentation, draft SOPs, implement quality management, and provide regulatory guidance for biomedical intervention studies.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Access, Trello
3w
Save
Mark Applied
Hide
Social Science Research Professional 2
Stanford or New Jersey
$76k-$142k/yr RemoteFull Time
2+ YOEBA in social science and 2 years relevant experience (or equivalent); qualitative fieldwork, interviewing, transcription, analysis, IRB compliance, strong writing and organizational skills.
3h
Save
Mark Applied
Hide
Clinical Research Coordinator I
Alameda, California, United States
$25-$30/hr HybridMultiple Commitments Available
Bachelor's degree in a related field; participant-facing communication, study scheduling, documentation, and logistics skills. GCP, IRB, or clinical study documentation familiarity is preferred but not required.
2mo
Save
Mark Applied
Hide
Senior Research Associate (Research Technician III, Range 1) - Office of Research and Sponsored Programs/Public Health
San Francisco or California
$67k-$71k/yr OnsiteFull Time, Temporary
Experience compiling, managing, and analyzing quantitative and qualitative research data; supervising small research teams; ensuring IRB compliance; strong written and oral communication and organizational skills.
EndNote, Microsoft Excel
1mo
Save
Mark Applied
Hide
CLIN RSCH CRD
San Francisco or San Francisco
OnsiteFull Time
High school graduate with attention to detail, strong communication, ability to multitask, complete projects independently; familiarity with IRB/CHR systems, EMR, data tools and research regulations preferred.
Committee of Human Research (CHR) online iMEDris system, Microsoft Excel, Microsoft Access, Stata, SASS, SPSS, REDCap, Teleform, Microsoft Word, Electronic Medical Records (EMR)
2w
Save
Mark Applied
Hide
Director, Pharma Delivery Operations
Redwood City, California, United States
$215k-$245k/yr HybridFull Time
8+ YOEBachelor's required; 8+ years in clinical operations or delivery/program management; people management experience; client and contract management; working knowledge of GCP and IRB processes; strong analytical and communication skills.
Jira, Hubspot
3mo
Save
Mark Applied
Hide
Project Manager
Stanford, California, United States
$110k-$124k/yr HybridFull Time
4+ YOEBachelor's degree and 4 years clinical research experience (or equivalent). Must have research regulatory knowledge (HIPAA, FDA, IRB, GCP), Microsoft Office proficiency, project leadership, and medical terminology.
Microsoft Office
5d
Save
Mark Applied
Hide
Director, GCP Inspection Readiness and Audits Strategy
Princeton or South San Francisco
$194k-$250k/yr HybridFull Time
10+ YOEBachelor’s degree in life sciences or related field, 10+ years of clinical trials experience, and senior GCP inspection readiness and FDA BIMO experience. Requires sponsor, CRO, site, IRB, compliance, and audit expertise.
2mo
Save
Mark Applied
Hide
Clinical Research Coordinator
San Francisco, California, United States
OnsiteFull Time
2+ YOEManage end-to-end participant recruitment, maintain recruitment metrics, serve as participant contact, assist with adverse event reporting and clinical documentation, support IRB/regulatory submissions; bachelor’s in STEM and ~2 years experience preferred.
Good Clinical Practice (GCP)
1mo
Save
Mark Applied
Hide
Clinical Research Assistant – Mind Body Interventions for Chronic Pain & PTSD
Palo Alto, California, United States
$39/hr OnsiteFull Time
2+ YOEBachelor's degree or equivalent, 2 years healthcare experience handling sensitive health data and interacting with patients; knowledge of GCP/IRB/FDA/HIPAA; Microsoft Word/Excel proficiency; ability to manage multiple studies and regulatory submissions.
Microsoft Word, Microsoft Excel
1mo
Save
Mark Applied
Hide
Director, Clinical Research & Regulatory Affairs
San Francisco or New York City
$230k-$245k/yr HybridFull Time
7+ YOEBS in engineering or technical field required (advanced degree preferred); 7+ years in medical device/healthcare with ≥6 years in clinical affairs/clinical trial management; strong GCP, IRB, protocol, SOP, and KOL relationship experience; leadership skills.
Compass AI™, Butterfly Garden™, Ultrasound-on-Chip™, Software as a Medical Device (SaMD), AI/ML, Good Clinical Practice (GCP)
1w
Save
Mark Applied
Hide
Research Coordinator
Boston or United States or United Kingdom or Canada or London or Oakland or Burlington or Nahant or Arlington or Charlotte or Miami or Portland or Seattle or Toronto or Vancouver or Africa
$49k-$67k/yr OnsiteFull Time
Bachelor’s degree in psychology, neuroscience, public health, or related field; organizational and communication skills, independent work, and large-scale pediatric or clinical trial data experience required.
MATLAB, Python, R, Unix, bash, tsch, HTML, EEG, fMRI, IRB
3d
Save
Mark Applied
Hide
Director of Clinical Affairs
Boston or San Francisco
$200k-$250k/yr HybridFull Time
10+ YOE5+ MgmtRequires 10+ years of clinical operations experience, 5+ years in leadership, 7+ years of cross-functional program management, a bachelor's degree, and expertise in FDA-regulated medical device studies, clinical data, and regulatory compliance.
IRB, CRO, CRF, eCRF, FDA, 21 CFR, ICH-GCP, ISO 14155, SaMD, 510(k), RWE
3d
Save
Mark Applied
Hide
Human Neuroscientist, Intracranial Recording
Emeryville, California, United States
$120k-$220k/yr OnsiteFull Time
PhD or MD/PhD expected; human intracranial electrophysiology, cognitive paradigm design, quantitative analysis, Python or MATLAB, clinical collaboration, and advanced cognitive neuroscience expertise required.
Python, MATLAB, sEEG, ECoG, Utah array, microelectrode arrays, IRB
Explore Jobs
Expand Your Job Search
Top Cities Near San Francisco for Irb
- Irb jobs in San Jose, CA
- Irb jobs in Oakland, CA
- Irb jobs in Fremont, CA
- Irb jobs in Santa Rosa, CA
- Irb jobs in Hayward, CA
- Irb jobs in Sunnyvale, CA
- Irb jobs in Concord, CA
- Irb jobs in Santa Clara, CA
- Irb jobs in Vallejo, CA
- Irb jobs in Berkeley, CA
- Irb jobs in Fairfield, CA
- Irb jobs in Antioch, CA
- Irb jobs in Richmond, CA
- Irb jobs in Daly City, CA
- Irb jobs in San Mateo, CA
- Irb jobs in Vacaville, CA
- Irb jobs in San Leandro, CA
- Irb jobs in Livermore, CA
- Irb jobs in Redwood City, CA
- Irb jobs in Mountain View, CA