216 study manager jobs at 137 companies in Blackstone, MA
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Sr. Manager, Study Start Up
Cambridge or Boston
$140k-$190k/yr RemoteFull Time
8+ YOE5+ MgmtBachelor's degree in science or related field, 8+ years in multinational clinical studies, 5+ years managing clinical study operations, and global study start-up, site activation, CRO, GCP, and regulatory experience.
Key Performance Indicators (KPIs)
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.
3w
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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, study coordination, or related work; project management, communication, organization, problem-solving, and recruitment strategy skills required.
CRM, participant databases, scheduling platforms, research management software
2w
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Clinical Study Design Manager
Boston or Raleigh
OnsiteFull Time
3+ YOERequires 3+ years in clinical research or life sciences, 3+ years designing CRF/ePRO or clinical trial databases, 2+ years CRIO experience, and a health science bachelor's degree or equivalent.
CRIO, Microsoft Office, Google applications
3d
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Study Supply Manager
Boston, Massachusetts, United States
$98k-$147k/yr HybridFull Time
5+ YOEBachelor’s degree with 5+ years of relevant experience, or MS, PhD, or PharmD with 2+ years. Requires ICH GCP and regulatory knowledge, demand planning, forecasting, analytics, and advanced problem-solving.
2d
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Study Supply Manager
Boston, Massachusetts, United States
$98k-$147k/yr HybridFull Time
5+ YOEBachelor’s degree with 5+ years’ relevant experience, or MS, PhD, or PharmD with 2+ years. Requires ICH GCP and regulatory knowledge, demand planning, forecasting, analytical skills, and advanced problem-solving.
2d
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Study Supply Manager
Boston, Massachusetts, United States
$98k-$147k/yr HybridFull Time
5+ YOEBachelor’s degree with 5+ years, or MS, PhD, or PharmD with 2+ years relevant experience; knowledge of ICH GCP and regulatory requirements; demand planning, forecasting, analytical, and advanced problem-solving skills.
2w
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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
3w
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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
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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
1mo
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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.
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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.
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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
3w
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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
4w
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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, Clinical Operations Study Lead
Cambridge, Massachusetts, United States
$170k-$180k/yr OnsiteFull Time
7+ YOE2+ MgmtBachelor's in life sciences,7+ years clinical operations experience with 2+ years study/team leadership,experience with global trials,CTMS/eTMF/EDC,ICH-GCP/FDA/EMA knowledge,vendor and budget management.
CTMS, eTMF, EDC
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
1w
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Study Start Up Lead Contractor
Boston, Massachusetts, United States
RemotePart Time, Contract
8+ YOEBA/BS and 8+ years supporting or independently managing global clinical trials; strong ICH/GCP, regulatory, drug development, CRO/vendor oversight, communication, and cross-functional collaboration experience.
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
3w
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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
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