110 study manager jobs at 76 companies in Foster, RI
1mo
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Study Manager I (3910)
Brookline, Massachusetts, United States
$80k-$105k/yr OnsiteFull Time
5+ YOEEnsures regulatory-compliant clinical trial conduct at assigned sites, maintains study documentation, trains site staff, enforces safety reporting, and supports enrollment and data quality.
EDC, IVRS
1w
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Clinical Study Associate Manager
Armonk or Cambridge or Warren
$110k-$179k/yr OnsiteFull Time
4+ YOEBachelor's degree and 4+ years industry experience, clinical trial operations experience, knowledge of ICH/GCP, vendor management, budget awareness, and strong attention to detail.
CTMS, TMF, IVRS/IWRS, EDC, Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel
2w
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Interventional Study Scientist Medical Director
London or Waltham or Upper Providence
$187k-$312k/yr HybridFull Time
Advanced degree (MD/PhD/PharmD), substantial experience designing and leading interventional clinical studies, regulatory knowledge, strong communication and organizational skills.
2w
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RTSM Study Project Lead - Level 1
Wellesley or United States
RemoteFull Time
3+ YOE3+ years software application support experience in clinical trial support or equivalent; skills in customer service, troubleshooting, issue management, and problem resolution; bachelor's degree or relevant experience.
Prancer RTSM, JIRA, Natural language processing (NLP)
1w
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Senior Manager or Associate Director, Preclinical Safety Study Monitor
Watertown, Massachusetts, United States
$145k-$240k/yr OnsiteFull Time
7+ YOE3+ Mgmt7+ years nonclinical toxicology experience, 3+ years monitoring outsourced GLP studies, GLP knowledge, ability to lead CRO studies, strong communication and organizational skills, willingness to travel ~5–10%.
Veeva, Microsoft SharePoint
4w
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Director, Clinical Operations Study Lead
Cambridge, Massachusetts, United States
$202k-$214k/yr OnsiteFull Time
10+ YOE4+ MgmtBachelor's in life sciences,10+ years clinical operations experience with ≥4 years study/team leadership; experience with global trials, CTMS/eTMF/EDC, ICH-GCP, vendor management, budgeting and stakeholder communication.
CELL+GENE™, CTMS, eTMF, EDC
1mo
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Contractor (6 Months) Study Coordinator (equivalent level to RA)
Cambridge, Massachusetts, United States
$40-$45/hr OnsiteContract, Temporary
2+ YOEBS plus 2 years biotech experience; experience with Smartsheet, ThinkCell, sample management/shipping, LIMS (Benchling); preferred experience with in vivo studies, Microsoft Excel, and GraphPad Prism; strong organization and cross-functional communication.
Smartsheet, ThinkCell, LIMS, Benchling, Microsoft Excel, GraphPad Prism
3d
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Study Abroad Advisor
Waltham, Massachusetts, United States
$61k-$66k/yr OnsiteFull Time
3+ YOEB.A./B.S. required, M.A./M.S. preferred; 3-5 years relevant experience; knowledge of a second language; experience with Microsoft Office, Terra Dotta, and Workday preferred.
Microsoft Office, Terra Dotta, Workday
6d
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Senior Clinical Study Analyst
Cambridge, Massachusetts, United States
$85k-$95k/yr HybridFull Time
5+ YOEBachelor's degree or equivalent,5+ years clinical research or trial experience,experience with patient data/EMR,strong research,communication and client-management skills.
TriNetX LIVE™, EMR
1mo
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Associate Director, Regional Clinical Study Management
Malaysia or Basel or Beijing or Cambridge or Asia
RemoteFull Time
13+ YOE3+ MgmtBachelor or higher (life science preferred), 13+ years clinical research experience, 8+ years clinical operations/project management experience, 3+ years people management; expert knowledge of ICH-GCP; fluent English; PMP preferred.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Microsoft Teams, CTMS, EDC, eTMF
3w
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Director, Study Quality and Compliance - Nonclinical Safety/Toxicology
Cambridge, Massachusetts, United States
$186k-$345k/yr OnsiteFull Time
10+ YOEAdvanced degree in biological sciences with 10+ years (or BS with 15+ years), GLP and toxicology study experience, people management, SEND familiarity, strong communication and planning skills.
Smartsheet, SEND
1w
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Directed Study Paraprofessional
Easton, Massachusetts, United States
$18-$29/hr OnsiteFull Time
0+ YOESupervise grades 11–12 in directed study, monitor grades, support completion of academic/vocational work; proficiency with SchoolBrains and Google Classroom; strong communication, organization, and classroom management; work authorization required.
SchoolBrains, Google Classroom
4w
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Director, Study Quality and Compliance - Nonclinical Safety/Toxicology
Cambridge, Massachusetts, United States
$186k-$345k/yr HybridFull Time
10+ YOEAdvanced degree in biological sciences with 10+ years (or BS with 15+ years), GLP and toxicology experience, people leadership, SEND familiarity, and software/data management experience.
Smartsheet
1mo
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SENIOR FHS DATA MANAGER/ANALYST, School of Medicine, Framingham Heart Study
Framingham or Boston
$90k-$100k/yr HybridFull Time
3+ YOESenior technical lead for end-to-end data management, statistical programming, and data integration for the Framingham Heart Study; fluency in SAS and R; bachelor's with 5-7 years or master's with 3-5 years of related experience.
SAS, R
2mo
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Manager/Senior Manager, Trial Operations
Needham or Boston
$140k-$195k/yr HybridFull Time
5+ YOEMinimum 5-8 years clinical project/study management experience; bachelor’s degree in a scientific field; strong vendor management and cross-functional collaboration.
2mo
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Clinical Project Manager
Waltham, Massachusetts, United States
$130k-$150k/yr OnsiteFull Time
5+ YOE5+ years pharma/biotech experience including Clinical Study Lead; bachelor’s in health-related field preferred; strong clinical operations, ICH/GCP, project management, site selection/management, TMF and CRO oversight skills.
3w
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Senior Program Manager - Medical & Clinical Affairs
Bridgewater or Chicago or Washington or Boston or Atlanta or Orlando or Philadelphia or Lexington
RemoteFull Time
7+ YOEBachelor's in engineering or science preferred,7+ years managing technical projects in medical device/pharma,project management qualification preferred (PMP/APM),clinical study execution experience,strong communication and stakeholder management.
Microsoft Word, Microsoft Project, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams, database software, SAP, Microsoft Outlook, Project Management Cloud Software
1w
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Senior Clinical Trial Manager
Cambridge, Massachusetts, United States
OnsiteFull Time
5+ YOEBachelor's degree in life sciences or related field,5+ years clinical operations/study management experience in biotech,US site management,CRO oversight,GCP/ICH/FDA knowledge,oncology experience preferred,ability to travel (~25%).
3mo
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Senior Clinical Project Manager
Lexington, Massachusetts, United States
$160k-$180k/yr OnsiteFull Time
7+ YOEBachelor’s degree in health or biological science; 7+ years clinical operations with global trials; 3+ years as a clinical study lead or project manager; cardiovascular/rare disease experience preferred.
Electronic Data Capture (EDC), IRT, Clinical trial management software, Microsoft Office
1mo
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Senior Manager, Clinical Operations - Cardiology
Cambridge or Boston or New York City or Dallas or United States or Europe or India or Australia
$140k-$165k/yr HybridFull Time
8+ YOEBachelor's degree or equivalent, 8+ years supporting Phase II-IV clinical trials, deep knowledge of study startup/regulatory/GCP, stakeholder management, analytics, CTMS experience (RealTime preferred), and willingness to travel up to 30%.
CTMS, RealTime CTMS
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