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Associate Director, Clinical Development
Foster City, California, United States
HybridFull Time
3+ YOE3+ years pharma experience (2+ in clinical development), Bachelor's degree required (PhD/PharmD preferred), strong scientific writing, GCP/ICH knowledge, experience with CROs, clinical trial design and data review.
2w
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Vice President, Clinical Development – Inflammation
Foster City, California, United States
OnsiteFull Time
10+ YOEM.D. or M.D./Ph.D. required; 10+ years industry clinical development experience preferred; deep expertise in inflammation/immunology; global program and alliance leadership; strategic portfolio management and cross-functional leadership.
1mo
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Clinical Development Scientist
Palo Alto or Redwood City
$138k-$190k/yr HybridFull Time
5+ YOEAdvanced degree preferred, 5+ years post‑graduate industry experience, experience designing/managing clinical validation studies for IVDs and regulatory submissions, strong scientific writing and cross‑functional collaboration skills.
AI tools, NGS, GCP, GLP, CLIA, CAP, ISO 13485
1mo
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Associate Director, Clinical Biomarker Development
Redwood City, California, United States
$186k-$233k/yr HybridFull Time
3+ YOEPh.D. required; 3+ years clinical biomarker/assay development in industry; experience with assay development, validation and clinical implementation; CRO management; strong communication and independent problem-solving skills.
5d
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Assoc Clinical Development Director (MD)
Foster City, California, United States
$226k-$293k/yr HybridFull Time
MD/DO required; clinical development and medical monitoring experience preferred; familiarity with clinical trial design, regulatory guidelines (FDA/EMA/ICH/GCP), strong analytical and communication skills.
2mo
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Associate Director / Senior Manager, Clinical Development Program Manager
Redwood City, California, United States
OnsiteFull Time
7+ YOE7+ years drug development experience; 5+ years leading cross-functional teams; Bachelor's degree; advanced degree preferred; strong strategic leadership and communication.
Agile, Project Management Tools
4w
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Senior Director, Clinical Development
Foster City or Santa Monica or Parsippany
$255k-$364k/yr HybridFull Time
6+ YOEMD/DO with 6+ years drug development experience; board certification in hematology/oncology preferred; experience leading oncology clinical programs, regulatory interactions, and mentoring physicians.
1w
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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)
2w
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Clinical Project Manager
San Jose, California, United States
OnsiteFull Time
6+ YOEBachelor's required (Master's preferred); 6+ years clinical research experience preferred; 2-5 years as Senior CRA; experience running clinical studies, familiarity with FDA/ICH-GCP, project management and stakeholder communication.
3w
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Clinical Trial Manager
San Mateo, California, United States
$90-$135/hr OnsiteContract
10+ YOE3+ MgmtBachelor's in life sciences, 10+ years clinical operations, 3+ years leading trials, CRO/vendor oversight, knowledge of ICH-GCP/FDA/EMEA, GDPR, and experience across Phase 2/3 global trials.
EDC, IXRS, eCRF
1w
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Sr. Clinical Trial Manager
Los Gatos, California, United States
$140k-$180k/yr OnsiteFull Time
7+ YOE7+ years managing medical device clinical trials including start-up, monitoring oversight, and closeout; strong knowledge of ICH GCP, ISO 14155, and FDA regulations; experience with CROs, EDC, budgeting, and regulatory inspections.
EDC, eTMF, Smartsheet, Microsoft Project
4w
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Regional Clinical Operations Manager
Burlingame, California, United States
$125k-$175k/yr FieldFull Time
4+ YOE4+ years operations leadership, multi-site management experience, ability to travel regularly across Bay Area clinics, manager development skills, data/KPI-driven decision making, valid CA driver's license required.
2mo
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Manager of Clinical Research, AQMed
Palo Alto, California, United States
$131k-$246k/yr OnsiteFull Time
10+ YOE10+ years clinical research in medical devices/diagnostics; multi-center trials; IRB/EC submissions; regulatory coordination; CRO management; AI-forward clinical workflows.
AI tools
1mo
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Sr. Clinical Trials Manager - VahatiCor
Santa Clara or United States
$135k-$183k/yr RemoteFull Time
7+ YOEBachelor's in a life science/related field, 7+ years managing clinical studies in medical device (cardiovascular preferred), knowledge of FDA/ICH-GCP, study startup, vendor management, enrollment forecasting, and willingness to travel up to 30%.
5d
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Clinical Producer - Health
Cupertino, California, United States
OnsiteFull Time
Guide end-to-end development of health features and collaborate with cross-functional partners to build clinical products.
1mo
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Associate Medical Director, Clinical Development - Job ID: 1912, 1913, 1914
Palo Alto, California, United States
$255k-$265k/yr HybridFull Time
3+ YOEM.D. required; completion of residency/fellowship preferred; physician licensure and board certification preferred; ≥3 years industry experience and ≥2 years clinical trial design experience; strong communication and leadership skills.
TransCon
1mo
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Senior Manager, Clinical Data Management
Redwood City, California, United States
$171k-$201k/yr OnsiteFull Time
5+ YOE5+ years clinical data management experience in trials; bachelor’s or higher preferred. Experience with SAS, EDC (Rave/Medrio), CDISC/SDTM, vendor/CRO management, CDISC compliance, and relevant regulations (ICH, GCDMP, 21CFR Part 11).
SAS, Rave, Medrio, Tableau, RShiny, EDC, CDISC/SDTM
2w
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Senior Clinical Program Manager
Brisbane or Hayward
$175k-$190k/yr RemoteFull Time
8+ YOE7+ MgmtBachelor's preferred,8+ years industry experience with 7+ years global study management; oncology/immunology experience preferred; strong leadership, communication, and analytical skills; willing to travel 10–20%.
Microsoft Office, EDC, IRT, CTMS, eTMF
3d
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Clinical Coordinator
Sunnyvale, California, United States
OnsiteFull Time
Coordinate clinical and operational processes, maintain regulatory compliance, oversee documentation, manage staff development, and support patient care in a dialysis clinic.
1mo
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Sr. Director, Clinical Development
Palo Alto or Baltimore
HybridFull Time
8+ YOE6+ MgmtPhD or MD required; 8+ years leading clinical study design and development; 3–5 years IVD diagnostics experience; 6+ years management; knowledge of ICH E6(R3) GCP, ISO 14155, ISO 13485, 21 CFR Part 820; oncology preferred.
NLP, LLM, EHR, FAIR principles, FHIR-OMOP, Common Data Models
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