3mo
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Associate, Clinical Research
Irvine, California, United States
$75k/yr OnsiteFull Time
1+ YOE1 year clinical trial research experience; degree in biological sciences, pharmacy, or nursing preferred; proficient in clinical trial management and data capture.
Clinical trial management systems, Electronic data capture systems
1mo
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Clinical Research Associate II
Los Angeles, California, United States
$24-$36/hr OnsiteFull Time
1+ YOEHigh school diploma required; bachelor's in science or sociology preferred. 1+ year clinical research experience. Preferred SOCRA or ACRP certification. Experience with EDCs/CRFs, IRB submissions, GCP and HIPAA compliance, participant scheduling and data collection.
Electronic Data Systems (EDCs)
2mo
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Associate Director, Aesthetics Clinical Development
Irvine, California, United States
$142k-$269k/yr HybridFull Time
7+ YOEAdvanced degree preferred; 7+ years clinical development experience; aesthetics devices knowledge; regulatory submission experience; cross-functional leadership.
Clinical Trial Management System, Data Analysis, Office Suite
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
3w
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Associate Director, Clinical Science (Autoimmune)
Pasadena or San Diego
$171k-$209k/yr HybridFull Time
10+ YOEBS in life sciences required; PhD/PharmD/MS/RN preferred. Minimum 10 years pharmaceutical clinical development experience and 2 years in therapeutic area. Experience in protocol development, safety monitoring, data review, and use of EDC and analysis tools required.
Microsoft Office, Microsoft Visio, GraphPad Prism, Spotfire, Medidata RAVE, Electronic Data Capture (EDC)
2w
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Sr. Clinical Trials Associate - Onsite in Aliso Viejo, CA
Aliso Viejo, California, United States
$108k-$135k/yr OnsiteFull Time
5+ YOE5-8 years CTA experience in ophthalmic field, bachelor's in science preferred, ability to coordinate clinical trials, review and clean data, maintain study master file, support audits, and lead meetings.
2mo
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Sr Clinical Research Associate (CRA)
Irvine, California, United States
$110k-$153k/yr HybridFull Time
5+ YOEBachelor’s in life sciences; minimum 5 years CRA experience in ophthalmology; vendor oversight; knowledge of ICH/GCP; strong MS Office and data management skills.
MS Office, Excel, PowerPoint, Clinical trial software, EDC
3w
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Associate Director, Clinical Science (Autoimmune)
Pasadena or San Diego
$171k-$209k/yr HybridFull Time
10+ YOEBS in life sciences required; PhD/MS/PharmD/RN preferred. Minimum 10 years pharmaceutical clinical development experience and 2+ years focused in therapeutic area. Experience in IBD, protocol development, safety monitoring, data review, and publications required.
Microsoft Office, Microsoft Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform, EDC
2mo
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Clinical Research Coordinator,RN
Los Angeles, California, United States
$55-$70/hr OnsiteFull Time
2+ YOEAssociate's degree in Nursing; RN license; 2 years clinical research experience; oncology trials knowledge; data accuracy; multitasking; organizational; communication; GCP; MS Office; trial management software.
Microsoft Office, Clinical trial management software
1mo
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Clinical Review Specialist (White Memorial)
Los Angeles, California, United States
$90k-$134k/yr OnsiteFull Time
2+ YOEAssociate's/technical degree required; 2+ years in quality management, data abstraction, or healthcare analytics; CPHQ or CPPS required; RN preferred; experience with clinical registries and quality reporting.
1d
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Clinical Research Coord, I
Fountain Valley, California, United States
$37-$54/hr OnsiteFull Time
2+ YOEMinimum 2 years clinical research experience, associates required (bachelor's preferred). Must understand protocols, GCP/ICH/FDA regulations, strong data skills, Microsoft Office proficiency, valid driver's license, research/phlebotomy/CITI certifications preferred.
Microsoft Word, Microsoft Excel, Adobe Acrobat
1mo
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Assistant Clinical Research Coordinator
Inglewood, California, United States
$20-$26/hr OnsiteFull Time
High school diploma required (associate preferred); basic clinical research knowledge; MA or phlebotomy and CPR/BLS preferred; experience in research/healthcare, GCP/HIPAA knowledge, and proficiency with electronic data capture, CTMS, and Microsoft Office preferred.
electronic data capture systems, clinical trial management software, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
1w
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Associate Medical Director - Clinical Informatics
Gardena, California, United States
$142k-$348k/yr OnsiteFull Time
5+ YOE5+ MgmtMD/DO with active CA license, Epic Builder Certification, board certification in Family/Internal/Med-Peds, 5+ years primary care and leadership experience, knowledge of Epic/EHR and data systems.
Epic, EHR
1mo
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Clinical Associate Professor of Family Medicine (Practitioner)
Los Angeles, California, United States
$240k-$290k/yr OnsiteFull Time
2+ YOE2+ MgmtCompleted residency and board certified or board eligible in Family Medicine, eligible for California medical licensure, minimum 2 years primary care leadership/clinical administration, experience supervising faculty, quality improvement and data-driven practice management.
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
2mo
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Research Associate - Computational Immunology
Los Angeles, California, United States
$71k-$89k/yr OnsiteFull Time
3+ YOEDevelop computational tools and pipelines for genomic immunogenomics analyses; analyze multi-omics data; collaborate with wet-lab and clinical teams.
Python, R, HPC, Docker, Singularity, SLURM
1w
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Associate Director of Stats Programming
Irvine, California, United States
$137k-$236k/yr HybridFull Time
8+ YOE3+ MgmtBachelor's in Statistics/Computer Science or related, 8+ years clinical research programming experience (medical device/pharma), 3+ years supervisory experience, strong SAS and R skills, CDISC/ADaM/SDTM familiarity, excellent communication.
Base SAS, SAS/STAT, SAS Macro, R, ADaM, SDTM, CDISC
1w
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Associate Director of Stats Programming
Irvine, California, United States
$137k-$236k/yr HybridFull Time
8+ YOE3+ MgmtBachelor's in statistics/CS or related, ≥8 years clinical research programming experience (medical devices/pharma), ≥3 years supervisory experience, strong SAS and R proficiency, CDISC experience preferred, excellent communication and leadership skills.
SAS, SAS/STAT, SAS Macro, R
1w
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Associate Director of Stats Programming
Irvine, California, United States
$137k-$236k/yr HybridFull Time
8+ YOE3+ MgmtBachelor's in statistics/computer science or related, 8+ years clinical research programming experience (medical device/pharma), 3+ years supervisory experience, strong SAS and R skills, CDISC/ADaM/SDTM knowledge, leadership and communication skills.
SAS, SAS/STAT, SAS Macro, R, CDISC, ADaM, SDTM
2mo
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Business Technology Solutions Associate Consultant - Risk-Based Quality Management (RBQM)
South San Francisco or Thousand Oaks or New York or Princeton or Philadelphia or Boston
$118k-$133k/yr HybridFull Time
3+ YOEBachelor’s or Master’s in related field; 3+ years delivering tech-enabled solutions; RBQM exposure; data concepts; Python exposure; clinical trial/process understanding; strong communication and leadership.
SQL, RDBMS, Data Warehousing, Cloud Platforms, Python
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