1mo
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Study Project Manager II
Irvine, California, United States
$125k-$237k/yr HybridFull Time
8+ YOEBachelor's degree required; 8+ years clinical research study management; leadership and cross-functional experience; experience with drug/device/interventional studies and end-to-end study operations; familiar with ICH/GCP and clinical trial systems (EDC, IRT, CTMS, eTMF).
EDC, IRT, CTMS, eTMF
2w
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Manager Study Start-up
Aliso Viejo or San Clemente or Burlington or United States
$130k-$163k/yr OnsiteFull Time
8+ YOE8+ years clinical research experience in medical device/pharma; experience leading study execution, timelines, budgets, and cross-functional teams; strong knowledge of FDA regulations and GCP; risk management skills.
4w
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Clinical Study Operations Engineering Program Manager - Health
Sunnyvale, California, United States
OnsiteFull Time
Experience managing clinical study operations, CRO onboarding, recruitment strategy, analytics-driven insights, and international expansion for study recruitment.
2mo
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Director, Clinical Study Management
Jersey City or Millbrae
$203k-$221k/yr HybridAll Commitments Available
12+ YOE12+ years in clinical study management; oncology focus; leadership in matrix org; strong GCP/ICh knowledge.
3w
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Senior Global Clinical Study Manager
Durham or Phoenix or Gilbert or San Francisco or New York City or Indianapolis or Tampa or Rockville or Chicago or Dallas
$93k-$233k/yr OnsiteFull Time
5+ YOE2+ MgmtBachelor's in life sciences, 5+ years clinical research/monitoring (including 2 years study management), Phase III and oncology experience, ICH-GCP and FDA knowledge, global trial and financial management, stakeholder leadership.
Microsoft Office, CTMS, EDC
1mo
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Sr. Clinical Study Manager
Sunnyvale, California, United States
$152k-$218k/yr RemoteFull Time
5+ YOEExperience managing clinical and outcomes research for medical device trials, protocol and ICF development, GCP/ICH knowledge, 5+ years clinical research experience (or equivalent), ability to travel 25–40%, strong communication and leadership skills.
Electronic Data Capture (EDC)
3w
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(CW) Sr. Study Specialist
San Rafael or United States
HybridContract
Lead or contribute to site monitoring, vendor management, study documentation, TMF management, ClinicalTrials.gov updates, investigator training, and meeting support; BA/BS preferred or relevant experience in biotech/pharma.
DocuSign, ClinicalTrials.gov, Trial Master File (TMF)
1w
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Reserve Study Analyst Assistant
Clovis, California, United States
$52k-$64k/yr OnsiteFull Time
Valid driver’s license and reliable transportation; strong math, analytical, and organizational skills; ability to read plans, take measurements, document inspections, and communicate with clients.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Bluebeam
5d
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Associate Director Study Start-up
United States or Thousand Oaks
$182k-$213k/yr RemoteFull Time
7+ YOE3+ MgmtClinical trial start-up expertise with multi-year clinical execution experience and at least 3 years managing people; doctorate/master's/bachelor/associate/HS with corresponding years of clinical experience acceptable.
2mo
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SCI-CTO Study Start-UP Project Manager (Hybrid)
Stanford, California, United States
$86k-$100k/yr HybridFull Time
2+ YOEBachelor's degree and 2 years clinical research experience (or equivalent); knowledge of clinical trials data management, HIPAA/FDA/IRB/GCP, Microsoft Office and database applications; strong interpersonal and communication skills; thoracic clinical knowledge preferred.
Microsoft Office
1w
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Senior Case Study Proctor - 6385704
San Francisco, California, United States
$58-$68/hr OnsiteFull Time
2+ YOE2+ years experience, ability to follow detailed protocols, troubleshoot hardware sensors and software, manage secure data uploads, document issues, and communicate clearly to participants.
1w
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Study Abroad Coordinator - International Center
San Luis Obispo or Solano County
$66k-$74k/yr OnsiteFull Time, Temporary
3+ YOEBachelor's degree, 3+ years progressive student services experience, strong advising, program development, risk management, and customer service skills; able to work independently with faculty, staff, and students.
1w
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Director, Clinical Operations Study Start-Up
Palo Alto, California, United States
$203k-$253k/yr OnsiteFull Time
15+ YOE5+ Mgmt15+ years pharma/biotech experience with study start-up for global Phase 3 trials, 5+ years managerial experience, BA/BS (graduate degree preferred), strong regulatory, CTMS/eTMF, vendor oversight, and leadership skills.
eTMF, CTMS
1w
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Middle School Lunch and Study Hall Assistant
Pleasanton, California, United States
$18-$22/hr OnsitePart Time
High school diploma/GED, dependable and patient with students, able to supervise and manage behavior, stand and move across campus, maintain safety and orderly environment.
1mo
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Executive Director, Study Support & Oversight
Malvern or San Diego or United States
HybridFull Time
12+ YOE5+ MgmtBachelor's degree required; 12+ years clinical operations experience with 5+ years leadership; experience overseeing CROs/vendors, Phase 1–3 trials, ICH-GCP/FDA regulations, inspection readiness, and strong operational leadership.
4w
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Study Hall Rooftop Lounge Sales & Marketing Manager
Berkeley, California, United States
$80k-$85k/yr OnsiteFull Time
2+ YOE2+ years hotel/catering/event/restaurant sales experience; strong prospecting, negotiation, pipeline management and client communication skills; CRM and content-tool familiarity; flexible schedule and on-property presence required.
CRM, Delphi/FDC, CI/TY, Sertifi, Canva, CapCut
4w
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Study Hall Rooftop Lounge Sales & Marketing Manager
Berkeley, California, United States
OnsiteFull Time
Selling and closing wedding event business; managing wedding sales pipeline in CRM; conducting site tours; creating proposals and contracts; coordinating event execution; driving F&B and room revenue; supporting social media lead conversion.
CRM
2mo
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Manager, Biomarkers and Bioanalytical Operations
San Francisco, California, United States
$122k-$163k/yr HybridFull Time
2+ YOELead biomarker and bioanalytical operations across clinical studies; manage CROs; ensure GCP/GCLP compliance.
Central Labs, Biomarker Testing, Data Management Systems
1mo
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Clinical Program Manager
Santa Monica or Foster City or Parsippany
$165k-$214k/yr HybridFull Time
6+ YOEResponsible for leading clinical study execution, managing teams and budgets, overseeing CROs/vendors, authoring study documentation/SOPs, ensuring regulatory/GCP compliance; requires advanced degree or equivalent years of experience.
1mo
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Product Manager, Design
Pleasanton, California, United States
$105k-$125k/yr OnsiteFull Time
2+ YOE2+ years in product design/management or hybrid role; portfolio/case studies; proficiency with Figma and modern prototyping; fluent with AI tools across research/design; strong ownership, communication, and cross-functional collaboration skills.
Figma
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