48 clinical data manager jobs at 30 companies in Chula Vista, CA
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Clinical Data Manager
San Diego, California, United States
$110k-$120k/yr OnsiteFull Time
2+ YOEMinimum 2 years clinical data management experience, bachelor's in medical or scientific field, EDC/IRT/ePRO experience, EMR/data system design, knowledge of CDISC and 21 CFR Part 11, strong communication and analytical skills.
Microsoft Office Suite, EDC, IRT, ePRO, CDISC
1mo
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Director, Clinical Data Management
San Diego, California, United States
$195k-$240k/yr HybridFull Time
12+ YOE5+ MgmtBS in life/computer sciences or math, 12+ years related experience with 5+ years data management and 5+ years people management in pharma/biotech; knowledge of ICH/FDA/GCP, CDISC/STDM/MeDRA, and clinical trial data lifecycle.
CDISC, STDM, MeDRA, Word, PowerPoint, Excel
4d
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Principal Specialist, Clinical Data Management
San Diego, California, United States
$131k-$179k/yr OnsiteFull Time
8+ YOE3+ MgmtRequires a computer science or related degree and 4–8+ years of pharmaceutical experience depending on degree, or 3+ years in a supervisory or lead capacity; expertise in clinical data management, CDISC standards, Medidata Rave, and Microsoft Office.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Medidata Rave, MedDRA, WHO Drug, CDISC, CDASH, SDTM, Business Objects, SAS
2w
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Director, Clinical Data Management
San Diego or United States
$201k-$263k/yr HybridFull Time
10+ YOEBachelor’s or Master’s in a relevant field, 10+ years of pharmaceutical, biotech, or CRO data management experience, oncology expertise, CRO oversight, EDC experience, and demonstrated team or vendor leadership.
Medidata RAVE, Veeva, Electronic Data Capture (EDC), Artificial Intelligence (AI)
3w
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Associate Director, Clinical Data Management
San Diego, California, United States
$190k-$205k/yr OnsiteFull Time
10+ YOE5+ Mgmt10+ years clinical data management experience with 5+ years leadership; expertise in EDC (Medidata Rave), CDISC standards, vendor management, regulatory submissions; BS required, advanced degree preferred.
Medidata Rave, CDISC CDASH, CDISC SDTM, ICH GCP E6(R3), 21 CFR Part 11
1w
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Director, Clinical Data Management
San Diego or Pasadena
$195k-$240k/yr HybridFull Time
12+ YOE5+ MgmtBachelor's degree in life, computer, or mathematical sciences; 12+ years related experience, including 5+ years clinical data management and people management in pharma or biotech; clinical trial lifecycle expertise.
CDISC, STDM, MedDRA, Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Electronic Data Capture (EDC)
3mo
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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
2w
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Director, Clinical Data Management
San Diego or United States
$201k-$263k/yr RemoteFull Time
10+ YOEBachelor’s or master’s degree required; 10+ years of pharmaceutical, biotech, or CRO data management experience; oncology expertise, CRO oversight, EDC, GCP, CDISC/CDASH, ICH, FDA, and AI-tool experience required.
Medidata RAVE, Veeva, Electronic Data Capture (EDC), Artificial Intelligence (AI)
1mo
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Clinical Marketing Manager
San Diego, California, United States
$120k-$165k/yr OnsiteFull Time
5+ YOEBachelor's degree required,5+ years clinical marketing/medical affairs experience in medtech/pharma,ability to translate clinical data,conference/CME strategy experience,travel up to 30%,proficiency with Microsoft Office; HubSpot/Salesforce a plus.
Microsoft Office Suite, HubSpot, Salesforce
2mo
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Clinical Research Manager
Escondido, California, United States
$100k-$105k/yr OnsiteFull Time
5+ YOE5+ years as a delegated CRC on multiple phase 2-4 trials, proficiency with FDA regulations, supervisory experience, data management and documentation skills, knowledge of medical terminology, IATA and GCP.
CTMS
1d
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Data Scientist - Hybrid - 140926
San Diego or La Jolla
$140k-$180k/yr HybridFull Time
5+ YOERequires 9 years related experience or bachelor's degree plus 5 years relevant experience, advanced HPC/data science/CI expertise, Python, TensorFlow, PyTorch, Matlab, cloud computing, AI clinical decision support, and healthcare data exchange protocols.
Python, TensorFlow, PyTorch, Matlab, Amazon Web Services (AWS), Google Cloud Platform (GCP), HPC, CI
1w
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Senior Manager, Clinical Scientist, Translational Science & Medicine-Immunology
Spring House or San Diego or Cambridge or Leiden
$137k-$274k/yr HybridFull Time
6+ YOEBachelor’s degree in a scientific discipline and 6–9 years of clinical research experience required. Requires clinical development, trial design, regulatory, GCP, data analysis, communication, and project management expertise.
Microsoft Office Suite, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, clinical trial management software, generative artificial intelligence, Good Clinical Practice (ICH/GCP)
3mo
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Clinical Research Coordinator
San Diego, California, United States
$70k-$80k/yr OnsiteFull Time
Medical Oncology Associates of San Diego: Provides specialized oncology and hematology treatment and care services.
1+ YOECoordinate clinical studies, screen patients, obtain consent, manage data, ensure GCP/IRB compliance, and assist with enrollment and reporting.
Good Clinical Practice (GCP), Case Report Forms (CRFs), IRB documentation, Sponsor query response systems
2w
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Director, Data, Data Science and Artificial Intelligence – Oncology / Bladder Cancer
Spring House or New Brunswick or Cambridge or Raritan or Titusville or San Diego
$164k-$283k/yr OnsiteFull Time
8+ YOEAdvanced degree in a data-intensive field, 8+ years in drug development or related disciplines, oncology and clinical trials knowledge, AI/ML and advanced analytics experience, healthcare datasets expertise, and partnership leadership.
R, Electronic Health Records (EHR), Machine Learning (ML), Artificial Intelligence (AI)
1mo
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Director, Clinical Development Scientist (Non-MD)
Collegeville or La Jolla or Lake Forest or Cambridge or Groton or New York City
$177k-$294k/yr HybridFull Time
5+ YOELead clinical execution, provide clinical and safety guidance, support protocol design and data review, manage committees, and may supervise clinical colleagues; requires substantial clinical research experience in biopharma.
3w
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Marketing Manager, Clinical Marketing & Sales Enablement
Carlsbad, California, United States
$120k-$160k/yr OnsiteFull Time
5+ YOEBachelor's degree and 5+ years healthcare/diagnostics/biotech marketing experience; clinical content and sales enablement experience; strong writing, project management, and cross-functional collaboration; ability to interpret clinical data.
3mo
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Vice President, Clinical Development
San Diego, California, United States
$345k-$375k/yr OnsiteFull Time
10+ YOE5+ MgmtExecutive-level clinical development leader; 10+ years in biotech/pharma with leadership of multi-program development and regulatory submissions.
Clinical development, Biometrics, Medical writing, Regulatory submissions, Data analysis
1w
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Program Manager Clinical, Consultant (Small To Mid)
Long Beach or California or El Dorado Hills or Lodi or Oakland or Rancho Cordova or Redding or San Diego or Woodland Hills
$112k-$167k/yr HybridFull Time
7+ YOEBachelor's degree or equivalent experience, 7+ years of relevant experience, current California LVN, RN, NP, or PA license, project management, healthcare data analysis, communication, and cross-functional leadership skills.
Microsoft PowerPoint
3mo
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Clinical Research Associate, Sponsor Dedicated
Carlsbad or Durham or Overland Park or Parsippany
$64k-$189k/yr FieldFull Time
2.5+ YOE2.5 years site-level clinical research coordination experience, nursing or university (bachelor) degree, knowledge of electronic data capture preferred, ability to perform site monitoring and regulatory management.
Electronic data capture
1w
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Senior Mrg/Associate Dir, Clinical Science
San Diego or United States
$182k-$196k/yr HybridFull Time
6+ YOEBachelor's degree and 6+ years in life sciences or equivalent experience; clinical data analysis, protocol development, GCP and regulatory knowledge, cross-functional collaboration, and strong analytical skills required.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Electronic Data Capture (EDC), RAVE, J-Review, CTCAE, MedDRA, GCP, ICH, FDA, EMA
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