88 clinical study manager jobs at 37 companies in San Jose, CA
4w
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Senior Clinical Study Manager
Sunnyvale, California, United States
$152k-$218k/yr HybridFull Time
5+ YOEExperience managing multi-center premarket and post-market clinical studies, protocol/ICF development, GCP knowledge, literature review, contract/budget negotiation, team leadership, and 5+ years clinical research experience or equivalent.
Electronic Data Capture (EDC)
1mo
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Senior Global Clinical Study Manager
Chicago or Dallas or Durham or Gilbert or Indianapolis or New York or Phoenix or Rockville or San Francisco or Tampa
$93k-$233k/yr RemoteFull Time
5+ YOE2+ MgmtBachelor's in life sciences,5+ years clinical research experience including 2+ years clinical study management; oncology and global trial experience; knowledge of ICH-GCP, regulatory requirements, financial management.
Microsoft Office, CTMS, EDC
1mo
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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.
1mo
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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
3w
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Associate Director, Clinical Study Management, EMEA/LATAM
Jersey City or Millbrae
$183k-$221k/yr HybridFull Time
10+ YOE10+ years related experience (or 8 with postgrad), Bachelor’s degree required, deep knowledge of ICH-GCP and regional regulations, ability to manage global oncology/neuroscience trials, budget/resource management, strong leadership and communication.
Veeva TMF
1w
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Global Study Director
South San Francisco, California, United States
OnsiteFull Time
7+ YOE3+ MgmtUniversity degree in medical, biological, or clinical research sciences; 7+ years of clinical trials; 3+ years of global study and team leadership; hematology/oncology expertise; project management and ICH-GCP knowledge.
Project management software
1w
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Participant Recruitment & Study Startup Manager
Chadds Ford or San Jose or Boston or Cambridge
OnsiteFull Time
Experience in participant recruitment, human factors, clinical or market research, study coordination, or related work; project management, communication, organization, problem-solving, and recruitment strategy skills required.
CRM, participant databases, scheduling platforms, research management software
2mo
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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.
1w
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Global Study Director
South San Francisco, California, United States
OnsiteFull Time
7+ YOE3+ MgmtUniversity degree in medical or biological sciences or related clinical research discipline; 7+ years of clinical trial experience, including 3+ years leading global studies and teams; hematology/oncology expertise required.
Project management software solutions
1w
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Global Study Director
South San Francisco, California, United States
OnsiteFull Time
7+ YOE3+ MgmtRequires a university degree in medical, biological, or clinical research-related sciences, 7+ years of clinical trial experience, 3+ years of global study and team leadership, hematology/oncology expertise, and ICH-GCP knowledge.
3mo
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Clinical Trial Manager
Campbell, California, United States
$136k-$152k/yr HybridFull Time
5+ YOE1+ Mgmt5+ years of clinical research management, preferably in medical devices; IDE studies; FDA/GCP knowledge; strong collaboration and communication; willingness to travel 20-30%
Clinical Data Management Systems, Regulatory Compliance, GCP, FDA Regulations, IDE
3mo
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Clinical Program Manager
Redwood City, California, United States
$143k-$178k/yr OnsiteFull Time
8+ YOE4+ MgmtRN or Bachelor’s or Masters in biological sciences or health-related field; 8+ years clinical operations experience; 4+ years cross-functional study management; strong FDA/ICH/GCP knowledge; CRO/vendor management; leadership in fast-paced settings.
1mo
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Sr Clinical Trials Manager
Foster City, California, United States
$158k-$204k/yr OnsiteFull Time
4+ YOEBA/BS +6 yrs or MA/MS +4 yrs relevant clinical/life sciences experience; comprehensive knowledge of FDA/EMA/ICH/GCP; experience leading clinical studies, CRO/vendor oversight, and people leadership; ability to travel as needed.
1mo
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Manager, Clinical Operations
Alameda, California, United States
$145k-$200k/yr HybridFull Time
8+ YOEBachelor's in a scientific field, 8+ years clinical research experience in medical devices (or 5+ with advanced degree), 2+ years monitoring experience, experience managing clinical operations teams, GCP and global study experience.
1mo
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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; knowledge of clinical trials data management, regulatory requirements (HIPAA,FDA,IRB,GCP), medical terminology, Microsoft Office; supervisory experience.
Microsoft Office
2w
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Clinical Program Manager, Early Phase Virology
Foster City, California, United States
$182k-$236k/yr HybridFull Time
6+ YOE4+ MgmtBA/BS or advanced degree with 6–8+ years clinical life‑sciences experience, 4+ years cross‑functional study management, CRO oversight, RFP development, GCP/FDA/EMA knowledge, leadership and communication skills.
1w
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Senior Clinical Trial Manager
South San Francisco or United States
$177k-$229k/yr HybridFull Time
8+ YOEUndergraduate scientific or health-related degree; 8+ years relevant experience including 5 years clinical pharmaceutical experience and 3 years study management. Requires global collaboration and regulatory knowledge.
Electronic Data Capture (EDC), IxRS, electrocardiogram (ECG), Trial Master File (TMF), Clinical Trial Management System (CTMS), Request for Proposal (RFP)
3mo
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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
3w
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Clinical Research Coordinator
San Francisco, California, United States
HybridFull Time
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
2mo
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Director of Clinical Studies
San Francisco or California
$223k-$248k/yr HybridFull Time
3+ YOELead clinical study coordination and governance for microbiome products; 3+ years clinical trial coordination; GCP familiarity; regulatory knowledge.
Qualtrics, Electronic Data Capture, Asana, Jira
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