2w
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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
2w
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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.
1mo
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Senior Manager, Preclinical Study Management
United States or Cambridge
$145k-$196k/yr HybridFull Time
8+ YOEPh.D. preferred; B.S. in biology/toxicology with 8+ years biotech/CRO experience. Experience managing outsourced GLP/non-GLP preclinical studies, CRO oversight, protocol development, budgeting/forecasting, knowledge of ICH/GLP/OECD, Smart Sheets proficiency.
Smart Sheets
1d
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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
1mo
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Senior Manager, Preclinical Study Management (Cambridge, MA, US, 02142)
Cambridge, Massachusetts, United States
$145k-$196k/yr HybridFull Time
8+ YOEPh.D. preferred; B.S. in biology/toxicology with 8+ years industry/CRO experience; experience managing outsourced preclinical (GLP/non-GLP) studies, CRO oversight, knowledge of ICH/GLP/OECD, Smart Sheets, strong communication and organizational skills.
Smart Sheets
19h
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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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Global Study Director (Cell Therapy)
Boston, Massachusetts, United States
$172k-$257k/yr HybridFull Time
7+ YOE3+ MgmtUniversity degree in medical/biological sciences, 7+ years clinical trial experience, 3+ years global study/team leadership, ICH-GCP knowledge, project management experience, strong communication and mentoring skills.
2w
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Global Study Director (Cell Therapy)
Boston, Massachusetts, United States
$172k-$257k/yr HybridFull Time
7+ YOE3+ MgmtUniversity degree in medical/biological sciences, 7+ years clinical trial experience with 3+ years global study/team leadership, ICH-GCP/regulatory knowledge, project management experience, stakeholder and vendor oversight skills.
5d
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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.
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
1d
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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)
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
1mo
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PROGRAM MANAGER, Study Abroad
Boston, Massachusetts, United States
$60k-$65k/yr OnsiteFull Time
3+ YOEBachelor's degree required (Masters preferred); 3+ years higher education experience with study abroad admissions emphasis; Microsoft Office and database/WordPress experience; strong advising, presentation, and organizational skills; occasional travel.
Microsoft Office, WordPress
3w
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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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Associate Director, Clinical Operations Study Lead
Waltham, Massachusetts, United States
$159k-$195k/yr OnsiteFull Time
8+ YOEUndergraduate degree in a scientific/health discipline, 8+ years clinical trial management (Phase I-III) with sponsor/CRO experience, CRO/vendor oversight, ICH/GCP knowledge, budget and TMF oversight, strong communication and leadership.
1w
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Clinical Study Delivery Lead, Global Clinical Operations, Oncology Therapy Area, R&D, Orion Corporation
Cambridge, Massachusetts, United States
$140k-$230k/yr HybridFull Time
10+ YOE5+ Mgmt10+ years clinical operations experience with 5+ years leading global oncology studies; Master's preferred; experience with FIH through Ph2/3, CRO management, budgets, GCP/ICH, and inspection readiness.
2mo
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Director, Study Start-Up
Watertown, Massachusetts, United States
$195k-$275k/yr OnsiteFull Time
10+ YOE10+ years in biotech/pharma with Clinical Operations project management; strong regulatory, ICH-GCP, process improvement, and cross-functional leadership.
GCP, Regulatory systems, Contract management
1w
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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
1w
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Corporate Work Study Program Office Manager
Lawrence, Massachusetts, United States
$50k-$60k/yr OnsiteFull Time
2+ YOEBachelor's degree preferred, 2 years relevant experience preferred, proficiency in Microsoft Suite, bilingual English/Spanish, strong communication, organization, confidentiality, and multitasking skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1mo
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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.
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