2mo
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Associate Director, Clinical Data Systems and Informatics
San Diego or San Mateo
$155k-$190k/yr OnsiteFull Time
7+ YOE2+ Mgmt7+ years clinical data management; hands-on and oversight; strong SQL; DBT; EDC/CDM experience; data quality emphasis; regulatory and standards familiarity; Python preferred.
SQL, DBT, Python, EDC, eCRF, Medrio, CDASH, CDISC, GCP
1mo
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Associate Director/Director, Clinical Data Management (San Mateo, CA, US)
San Mateo, California, United States
$162k-$240k/yr OnsiteFull Time
12+ YOE5+ MgmtLead data management strategy; oversee CROs; ensure regulatory compliance; Medidata Rave expertise; 12+ years in CDM with leadership.
Medidata Rave, RTSM, eCOA, Coder, eTMF, RIM, CDISC, CDASH
2d
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Clinical Research, Associate I
Alameda, California, United States
$74k-$116k/yr OnsiteFull Time
0+ YOEEnsure quality and integrity of clinical trial data, perform and coordinate internal clinical studies, conduct site monitoring, maintain trial documentation, and support regulatory readiness.
eTMF, Microsoft Suite
2mo
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Associate Director/Senior Manager, Data Science (Statistical Programming)
South San Francisco, California, United States
$180k-$220k/yr HybridFull Time
8+ YOELead data science activities for clinical development; SAS/R/Python; CDISC (SDTM/ADaM); pharma/biotech regulatory submissions; leadership for Senior Manager/Associate Director roles.
SAS, R, Python, CDISC, Shiny, Plotly, RWE
2d
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Clinical Research, Associate I
Alameda, California, United States
$74k-$116k/yr OnsiteFull Time
0+ YOEEnsure quality and integrity of clinical trial data, perform monitoring and site management, coordinate internal studies; BS in life sciences preferred; 0-1 years CRA/CRC/CTA experience; knowledge of CFR and ICH-GCP.
Microsoft Suite, eTMF
1w
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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.
2mo
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Clinical Research Associate, Sponsor Dedicated
Durham or Aurora or San Fernando or Clinton or Mansfield or Santa Cruz or Santa Fe or South Shore or Elk Grove or Hudson or Englewood or Bellingham or Marysville or Overland Park or Evanston or La Habra or Prescott or Westchester or Mount Vernon or Warren or Linden or Fremont or Del Mar or Lake Tahoe or Northfield or Fort Pierce or Wilkes Barre or Camden or Lancaster or Clarksville or Adair or Fort Collins or Breckenridge or Littleton or Liverpool or Ft Lauderdale or Springfield or Long Island or Gloucester or West Point or O'Fallon or Cheyenne or Manhattan or New City or Parsippany or Queens or New York City or Escondido or Oak Brook or Merritt Island or El Cajon or Ontario or Afton or Abilene or Orangevale or Abingdon or Orland Park or Shenandoah or Akron or Paradise Valley or Newark or Hollywood or Port Saint Lucie or Lawton or Portland or Chino Hills or Belmar or Sonora or Berkley or Springfield or Springfield or San Jose or Beverly Hills or Melbourne or Colorado Springs or St. Petersburg or Panama City or Redondo Beach or Crystal Lake or Rochester or Ada or Kansas City or Ainsworth or Carlsbad or Denver
$72k-$189k/yr OnsiteFull Time
2+ YOEMonitor sites, manage recruitment, ensure regulatory compliance and data quality across studies.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Mobile devices
1mo
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Associate Director, Global Clinical Scientist (Cell Therapy)
Brisbane or Princeton or Madison
$184k-$257k/yr HybridFull Time
5+ YOEDegree in life sciences preferred, 5+ years clinical science/research experience, proficient knowledge of GCP/ICH and clinical operations, strong medical writing and data review skills, leadership experience in clinical trials.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Electronic Data Capture (e.g., RAVE), RAVE, J-Review
1mo
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Clinical Research Coordinator Associate
Stanford, California, United States
$35-$44/hr HybridFull Time
2+ YOECoordinate moderately complex clinical studies, enroll and consent participants, collect specimens and data, maintain regulatory compliance, manage databases, and support monitor visits. Requires 2-year college + 2 years related experience or a Bachelor's degree; REDCap and Microsoft Office proficiency preferred.
REDCap, Microsoft Office
2mo
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Associate Director, Clinical Science - Inflammation and Immunology
Brisbane or Hayward or United States
$200k-$210k/yr HybridFull Time
5+ YOEDoctorate (PhD/MD/PharmD) or equivalent, 5+ years clinical scientist experience at pharma/CRO/biotech, experience in inflammation/immunology trials, data analysis, safety/pharmacovigilance, GCP and biostatistics knowledge, and line management experience.
3w
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Associate Director - Data Standards (Hybrid)
South San Francisco or North Chicago
$142k-$269k/yr HybridFull Time
12+ YOEBachelor's degree, 12+ years clinical research experience (10+ with a Masters), expert knowledge of CDISC standards (CDASH, SDTM, ADaM, define.xml), metadata repository experience, regulatory submission experience, and team leadership experience.
CDISC, CDASH, SDTM, ADaM, define.xml, BRIDG, ODM, SHARE, eCTD, metadata repository
1w
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Clinical Review Specialist (St. Helena)
Saint Helena, California, United States
$90k-$134k/yr OnsiteFull Time
2+ YOEAssociate degree in nursing/healthcare/HIM required, 2 years quality/data abstraction experience, CPHQ or CPPS required, RN preferred, experience with registries and quality reporting.
STS, CoC, NSQIP, E-Verify
1mo
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Associate Director, Statistical Programming
Redwood City, California, United States
$229k-$270k/yr OnsiteFull Time
10+ YOE10+ years clinical trial statistical programming experience, deep SAS and CDISC SDTM/ADaM knowledge, Pinnacle 21 experience, submission readiness, MS preferred, strong communication and independent problem-solving skills.
SAS BASE, SAS MACRO, SAS STAT, SAS GRAPH, SAS ACCESS, CDISC SDTM, CDISC ADaM, Pinnacle 21, Spotfire, Tableau, RShiny
3d
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Research Nurse III, Clinical Trials - San Francisco
San Francisco, California, United States
$162k-$209k/yr OnsiteFull Time
2+ YOECalifornia RN license required; 2+ years clinical healthcare experience (or 4+ with associate); BLS; clinical research protocol, data collection, and regulatory compliance experience.
1mo
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Associate Principal Biostatistician Clinical Safety Statistics (CSS)
North Wales or San Francisco or Los Angeles or Puerto Rico
$142k-$224k/yr HybridFull Time
3+ YOEPhD in statistics/biostatistics (3+ yrs) or Master’s (6+ yrs). Expertise in safety data, clinical trial design, SDTM/ADaM, survival/meta/Bayesian methods, SAS/R/R-Shiny, and strong communication and project skills.
SAS, R, R-Shiny, SDTM, ADaM
1mo
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Staff Research Associate
San Francisco, California, United States
OnsiteFull Time
HS diploma or equivalent with relevant experience; strong attention to detail, communication, multi-tasking; familiarity with EMR, data management, and regulatory compliance for clinical research.
Electronic Medical Records (EMR), Access, Stata, SASS, SPSS, Teleform
2mo
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Staff Research Associate II
San Francisco, California, United States
$25-$41/hr OnsiteFull Time
2+ YOEBachelor's in a related field; 2–3 years research/clinical trial experience; strong organization and communication; experience with psychophysiology, sleep data, and data analysis preferred.
Biopac, LSL, EEG, EDA, EMG, HRV, Facial Coding, PPG, MATLAB, Python, R
2d
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Associate Principal Statistical Analyst
Redwood City, California, United States
$164k-$205k/yr HybridFull Time
10+ YOE10–14 years statistical programming experience in biotech/pharma, CDISC (SDTM/ADaM/define.xml) knowledge, clinical trial programming and QC, BS/BA in a relevant field, leadership and multi-tasking skills.
SDTM, ADaM, define.xml
3mo
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Decision Analytics Associate Consultant - Biometrics
South San Francisco or Princeton
$118k-$133k/yr HybridFull Time
2+ YOEBachelor’s or master’s in quantitative or life sciences; 2-4 years in clinical data management/biometrics or analytics; strong data lifecycle and standards knowledge; EDC experience; SAS/R/Excel skills; client-facing mindset.
R, SAS, Excel, EDC (Medidata Rave)
2mo
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Staff Research Associate II
San Francisco, California, United States
$25-$41/hr OnsiteFull Time
2+ YOEBachelor’s in psychology, neuroscience, biology, public health, social work; 2–3 years in research/clinical trials; strong organization and communication; experience with psychophysiology, sleep, and data analysis preferred.
Biopac, Lab Streaming Layer, MATLAB, Python, R, EEG, actigraphy, EDA, EMG, HR, HRV, facial coding, remote PPG from video
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