188 study manager jobs at 123 companies in Hingham, MA
1mo
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Manager Study Start-up
Aliso Viejo or San Clemente or Burlington or United States
$130k-$163k/yr OnsiteFull Time
8+ YOE8+ years clinical research experience in medical device/pharma; experience leading study execution, timelines, budgets, and cross-functional teams; strong knowledge of FDA regulations and GCP; risk management skills.
2d
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Participant Recruitment & Study Startup Manager
Chadds Ford or San Jose or Boston or Cambridge
OnsiteFull Time
Experience in participant recruitment, human factors, clinical or market research, research operations, or study coordination; project management, communication, organizational, planning, and problem-solving skills required.
CRM, participant databases, scheduling platforms, research management software
1w
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Clinical Study Operations Manager
Boston or New York City or Paris
$90k-$110k/yr RemoteFull Time
Experience in clinical project/operations, strong project management and communication, familiarity with GCP/ICH and decentralized data collection, attention to detail, ability to manage multiple priorities.
Zendesk, Asana
5d
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Director, Study Lead (ClinOps)
Boston or San Diego
HybridFull Time
10+ YOE5+ Mgmt10+ years clinical operations experience with 5+ years leading global Phase II/III studies, CRO oversight, ICH‑GCP knowledge, cross‑functional leadership, budget and resource management.
eCOA, IRT, TMF
1d
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Global Study Lead
United States or Philadelphia or Cambridge
$145k-$196k/yr HybridFull Time
7+ YOE3+ MgmtRequires a bachelor's degree, 7+ years of clinical research experience, 3–5 years leading global trials, Phase 3 experience, CRO oversight, leadership, project management, and MS Office/MS Project proficiency.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Project
2w
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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
2d
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Global Study Lead
Cambridge or Philadelphia
$145k-$196k/yr HybridFull Time
7+ YOE3+ MgmtBachelor's degree, 7+ years of clinical research experience, and 3–5 years leading global Phase 1–4 trials including Phase 3 registrational studies. Requires CRO oversight, leadership, project management, and Microsoft Office and Project proficiency.
Microsoft Office Suite, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Project
2w
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Senior Study Management Specialist
Boston or New York City
$95k-$105k/yr HybridFull Time
2+ YOEMinimum 2 years study management/clinical trial coordination experience in US clinical research; degree in a scientific discipline; strong written communication, attention to detail, and knowledge of RWE and regulatory requirements.
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
1mo
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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
6d
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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
1w
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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
1mo
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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
2d
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Associate Director, Clinical Study Quality Lead (Hybrid)
Boston, Massachusetts, United States
$161k-$241k/yr HybridFull Time
8+ YOEBachelor's degree in a scientific or allied health field and 8+ years of relevant experience; expertise in ICH-GCP, global regulations, clinical trials, quality risk management, CAPA, metrics, and Microsoft Office.
Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Smartsheet, Visio, CAPA, ICH-GCP, FDA, EMA, MHRA
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
1mo
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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
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