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Clinical Study Manager
Fridley, Minnesota, United States
$110k-$160k/yr OnsiteFull Time
5+ YOELead clinical study execution and operations, site management, and data/regulatory compliance.
EDC systems, CTMS platforms, Clinical trial tracking tools
1mo
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Clinical Study Coordinator
Cleveland or Athens or Chattanooga
OnsiteFull Time
2+ YOE2+ years coordinating clinical research studies (or equivalent on-the-job training), GCP, IATA, and CPR required; phlebotomy and clinical research certification (ACRP/SOCRA) preferred; EDC data entry and site support experience.
EDC systems
1mo
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Clinical Study Manager
Plano, Texas, United States
OnsiteFull Time
3+ YOEBachelor’s in Life Sciences, Engineering, or related field; 3–8+ years clinical research; 2+ years medical device study management; ISO14155/FDA/GCP knowledge; EDC/CTMS/eTMF proficiency.
EDC, CTMS, eTMF
3d
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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)
4d
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Senior Clinical Study Administrator
Boston, Massachusetts, United States
$83k-$124k/yr OnsiteFull Time
3+ YOEBachelor's degree in life science, ~3 years clinical operations or study support experience, proficiency with MS Office, CTMS and eTMF, strong organization, communication, and collaboration skills.
Microsoft Excel, Microsoft Word, PowerPoint, CTMS, smartsheets, eTMF
2mo
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Clinical Research Study Manager
Tomball, Texas, United States
OnsiteFull Time
5+ YOE1+ MgmtLead clinical study operations, ensure protocol compliance, data quality, training, and site coordination.
2mo
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Director, Clinical Study Management
Jersey City or Millbrae
$203k-$221k/yr HybridAll Commitments Available
12+ YOE12+ years in clinical study management; oncology focus; leadership in matrix org; strong GCP/ICh knowledge.
2mo
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Clinical Study Coord
Duarte, California, United States
OnsiteFull Time
2+ YOEBachelor’s degree in Science, Health or related field; 2+ years of research or clinical experience; familiarity with FDA/GCP/ICH; strong organizational and communication skills.
EHR, Regulatory Compliance Software, Data Management Tools
1w
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Clinical Study Coordinator
Omaha, Nebraska, United States
$57k-$86k/yr OnsiteFull Time
2+ YOEBachelor's degree or equivalent, 2 years clinical or research experience, proficiency with Microsoft Excel/Word/Outlook, strong communication, organization, attention to detail, and computer literacy.
Microsoft Excel, Microsoft Word, Microsoft Outlook, Microsoft Access, EPIC One Chart
1w
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CLINICAL STUDY COORDINATOR
West Bend, Wisconsin, United States
$50k-$55k/yr OnsiteFull Time
1+ YOEAccredited college degree, 1+ year clinical research experience (or 2 years Phase I), BLS and ACLS (within first year), GCP knowledge, strong communication and organizational skills.
2w
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Clinical Study Coordinator
Austin, Texas, United States
$78k/yr OnsiteFull Time
3+ YOEBachelor's degree in a technical subject plus relevant experience (min 3 years) or advanced degree with experience; 1+ years clinical trials experience preferred; strong communication, organization, and Microsoft Office skills.
Microsoft Office
3w
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Clinical Study Manager
Rochester, New York, United States
$100k-$150k/yr RemoteFull Time
Bachelor's degree or equivalent, experience in clinical operations/drug-device development, ophthalmology experience preferred, knowledge of FDA/ICH/GCP/HIPAA/IRB, project management skills, strong communication and analytical abilities, Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft Teams, SurveyMonkey, Microsoft Forms, EDC, eCRF
1mo
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Senior Manager Clinical Study Lead (Clinical Experimental Sciences)
Cambridge or Armonk or Warren
$151k-$246k/yr OnsiteFull Time
8+ YOEBachelor's degree and 8+ years of relevant clinical experience; experience executing clinical studies, budgeting, vendor/CRO oversight, CTMS/TMF/SharePoint familiarity, and knowledge of SOPs and ICH/GCP.
Clinical Trial Management System (CTMS), Trial Master File (TMF), Microsoft SharePoint
3d
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Regional Clinical Study Associate Manager
United States
$96k-$131k/yr RemoteFull Time
Bachelor's degree in scientific or healthcare discipline required; experienced clinical operations professional able to manage regional study delivery, lead teams and vendors, ensure inspection readiness and compliance with ICH/GCP/SOPs.
3mo
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Clinical Nurse Study Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
Bachelor's degree and active RN license required. Perform/coordinate clinical procedures, administer medications, assess and document adverse events, screen/schedule subjects, and support study execution with Project Managers and Investigators.
1mo
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Clinical Study Documentation Specialist
Phoenix, Arizona, United States
OnsiteFull Time
2+ YOEAssociates degree; 2 years IRB document submission; strong clinical research documentation; proficient in Microsoft Office and regulatory systems; strong organization; able to manage multiple studies; background checks required.
Microsoft Office, IRB portals, CTMS, Regulatory systems
2d
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Senior Clinical Study Manager
United States
$120k-$150k/yr RemoteFull Time
6+ YOEBachelor's in life sciences/healthcare with 8+ years or Master's with 6+ years; knowledge of GCP and regulatory requirements, IHC and IVD study experience preferred, strong communication and project management skills.
2d
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Clinical Study Coordinator
New Orleans, Louisiana, United States
OnsiteFull Time
1+ YOEBachelor's degree,1+ year professional experience,strong organization,communication,EMR familiarity,and ability to manage vendors and trial documentation.
Electronic Medical Records (EMR)
1mo
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Senior Global Clinical Study Manager
Durham or Phoenix or Gilbert or San Francisco or New York City or Indianapolis or Tampa or Rockville or Chicago or Dallas
$93k-$233k/yr OnsiteFull Time
5+ YOE2+ MgmtBachelor's in life sciences, 5+ years clinical research/monitoring (including 2 years study management), Phase III and oncology experience, ICH-GCP and FDA knowledge, global trial and financial management, stakeholder leadership.
Microsoft Office, CTMS, EDC
3mo
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Clinical Nurse Study Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
Bachelor's degree, nursing license (RN); clinical experience in acute care setting preferred.
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