54 clinical trial manager jobs at 24 companies in Pasadena, CA
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Clinical Trial Manager
Huntington Beach, California, United States
$28-$40/hrOnsiteFull Time
National Institute of Clinical Research: Physician-owned U.S. clinical-trial management organization conducting multi-site studies for pharmaceutical and biotechnology sponsors.
7+ YOE3+ MgmtManage multi-site clinical trial operations, ensure regulatory compliance, supervise and mentor clinical staff, oversee CTMS/ETMF/EDC usage, and execute patient recruitment and study start-up through closeout.
Edwards LifesciencesNYSE: EW: Global leader in patient-focused innovations for structural heart disease.
8+ YOEBachelor's degree with related experience; preferred 8+ years in regulated industry and clinical trials; project management, CTMS and Microsoft Office proficiency; knowledge of ICH/GCP, ISO14155,21 CFR 820.
University of California, Irvine: Public land-grant research university and academic health system.
5+ YOEBachelor's degree or equivalent, 5+ years research experience, clinical trial management experience, people management, project management, strong communication and problem-solving; Clinical Trial Professional certification within one year.
Sr. Director, TA Lead - Trial Analytics, Insights, and Planning (TAIP)
Princeton or Cambridge or Arizona or Puerto Rico or Los Angeles County
$234k-$317k/yrHybridFull Time
Bristol Myers SquibbNYSE: BMY: Transforming patients' lives through science.
10+ YOE10+ years in management consulting, trial analytics, or clinical strategy; clinical trial feasibility and forecasting expertise; oncology experience; advanced degree preferred; proven global team leadership and stakeholder management.
forecasting models, dashboards, site feasibility tools
Syneos Health: Integrated biopharmaceutical solutions from lab to life.
2+ YOERequires 2–4 years of clinical trial experience, GCP/ICH and FDA/EMA knowledge, clinical systems and project management tools proficiency, and a relevant bachelor's degree or equivalent experience.
Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), electronic Trial Master File (eTMF)
Cedars-Sinai: Nonprofit academic medical center providing advanced healthcare and research.
3+ YOE5+ MgmtHigh school diploma/GED, 5 years of management or program/project management experience, and 3 years of related clinical research or industry experience required. Bachelor's degree and clinical trial operations experience preferred.
Hoag Memorial Hospital Presbyterian: A nonprofit regional health care delivery network.
3+ YOEBachelor's in finance/business/healthcare, 3+ years in clinical research operations/finance/accounting, knowledge of clinical trials, Medicare, GAAP, and proficiency with Microsoft Excel, ERP (Oracle), and CTMS.
Microsoft Excel, ERP, Oracle, Clinical Trial Management Systems (CTMS)
Syneos Health: Integrated biopharmaceutical solutions from lab to life.
2+ YOERequires 2–4 years of clinical trial experience, preferably in oncology or cell therapy, GCP/ICH and FDA/EMA knowledge, clinical systems proficiency, sponsor communication skills, and a relevant bachelor's degree or equivalent experience.
Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), electronic Trial Master File (eTMF)
Headlands Research: Multinational clinical trial site network conducting pharmaceutical research for diverse and specialty patient populations.
5+ YOE5+ years as a delegated Clinical Research Coordinator on multiple phase 2-4 trials; proficiency with FDA regulations, CTMS documentation, supervisory experience, and strong communication skills. IATA and GCP required.
Helios CR, Inc.: U.S. integrated clinical trial network serving patients, physicians, and biopharma sponsors with clinical research services.
6+ YOEOversee CRCs and RAs for oncology trials; ensure ICH-GCP/FDA/HIPAA compliance; manage study start-up, regulatory submissions, data quality, and budgets. Bachelor's preferred; CCRC and phlebotomy desired; 6+ years clinical research experience.
XencorNASDAQ: XNCR: Public clinical-stage biopharmaceutical developing engineered antibody medicines for patients with cancer and autoimmune diseases.
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)
Tarsus PharmaceuticalsNasdaq: TARS: Public biopharmaceutical developing and commercializing medicines for patients, initially focused on eye care.
10+ YOE8+ MgmtAdvanced science degree and 10+ years of biotech or pharmaceutical clinical development experience, including 8+ years of clinical trial leadership; regulatory, GCP, SOP, and people management expertise required.
Standard Operating Procedures (SOPs), Good Clinical Practice (GCPs), Statistical Analysis Plans (SAPs), Clinical Study Reports (CSRs), Investigator's Brochures (IBs)
City of Hope: Comprehensive cancer research and treatment organization.
2+ YOECoordinate oncology clinical trials including recruitment, informed consent, protocol execution, data management, and regulatory compliance. Requires bachelor’s degree (or substitute experience), minimum 2 years research/clinical experience, and various certifications within specified timeframes.
Santa Monica or Foster City or El Segundo or Parsippany
$115k-$164k/yrOnsiteFull Time
Kite Pharma: Kite is a Gilead-owned biopharmaceutical developing cancer immunotherapies for patients.
2+ YOEExperience in clinical research operations, interpretation of FDA/ICH guidelines, study start-up, document generation/review, vendor management, and metrics reporting. BS/BA +4yrs OR MS/MA +2yrs required; oncology clinical trial experience preferred.
Research Clinical Director-Psychiatric Pharm Clinical Research
Orange, California, United States
$185k-$225k/yrOnsiteFull Time
Pacific Neuropsychiatric Specialists: Private outpatient psychiatric group serving Southern California patients with medication management, psychotherapy, and advanced treatments.
2+ YOEDoctorate in a related field, 2+ years of clinical research experience including PI or subPI pharmaceutical trials, and knowledge of ICH-GCP, FDA regulations, and IRB processes.
Minnesota or Northridge or United States or California or Washington or District of Columbia or Massachusetts or New York City
$87k-$149k/yrHybridFull Time
MedtronicNYSE: MDT: Global leader in medical technology and healthcare solutions.
4+ YOEBachelor's degree and 4 years of relevant experience, or advanced degree and 2 years. Requires advanced EDC and clinical trial management systems knowledge, SQL, complex queries, and REST API development.
ImmunityBioNasdaq Global Select Market: IBRX: Public biotechnology developing and commercializing immunotherapies and vaccines for patients with cancer and infectious diseases.
7+ YOEBachelor’s degree, 7+ years in budget and contract development, 4+ years in clinical research, advanced Excel, clinical trial management systems, coverage analysis, and CPT coding experience.
Clinical Trial Management Systems, Microsoft Excel, Veeva CTMS, CPT
University of Southern California: Private research university based in Los Angeles.
0.5+ YOEExperience in clinical trials data management; data entry from medical records; regulatory compliance; sponsor coordination; data quality assurance.
Clinical Development Director, Early Development – Cardiometabolic/General Medicine
United States or Thousand Oaks
$275k-$372k/yrRemoteFull Time
AmgenNASDAQ: AMGN: Developing innovative medicines to fight serious diseases.
2+ YOEMD/DO with minimum 2 years research or industry experience; experience in early phase trials, clinical trial design, safety/PK review, and collaboration across functions.
Clinical Research Supervisor 1 - Hematology/Oncology
Los Angeles, California, United States
$89k-$190k/yrHybridFull Time
UCLA Health: Academic medical system providing comprehensive patient care and research.
5+ YOEBachelor’s degree and 5+ years of clinical research experience required. Requires regulatory, clinical trials budgeting, IRB/FDA, quality improvement, communication, organizational, and team leadership skills; master’s and clinical research certification preferred.