1w
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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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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 Clinical Study Manager
Providence or Raleigh or Minneapolis
$126k-$180k/yr OnsiteFull Time
5+ YOEBachelor's in health sciences; 5+ years clinical study planning; FDA/ISO documentation experience; ability to manage multiple priorities; strong organizational, analytical, and communication skills.
2w
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Study Supply Manager
Boston, Massachusetts, United States
$98k-$147k/yr HybridFull Time
5+ YOEDegree (Bachelor’s +5yrs or MS/PhD/PharmD +2yrs), knowledge of ICH GCP and regulatory requirements, demand planning/forecasting skills, advanced problem-solving, strong communication, flexibility for global hours.
2w
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Study Supply Manager
Boston, Massachusetts, United States
$98k-$147k/yr HybridFull Time
2+ YOEBachelor's with 5+ years or MS/PhD/PharmD with 2+ years; knowledge of ICH GCP and regulatory requirements; demand planning, forecasting and analytical skills; advanced problem-solving; strong communication; flexibility in working hours.
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
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
3w
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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
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
2w
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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.
6d
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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
1mo
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Program Manager
Charlestown, Massachusetts, United States
$80k-$116k/yr HybridFull Time
Mass General Brigham: Provides integrated medical care, research, and clinical training services.
5+ YOELead research operations, manage staff, build scalable systems, ensure regulatory compliance and timely study execution.
REDCap, OnCore, SOPs, Dashboards, Project Management Tools
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.
1mo
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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.
1mo
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(Senior) Program Manager - Toxicology
Boston or Suzhou or Nantong or United States or Europe
$110k-$130k/yr RemoteFull Time
2+ YOEPhD or MS in toxicology/pharmacology/DMPK (or related) with 2+ post-PhD years or 5+ post-MS years; experience with in vitro/in vivo studies; program management experience preferred; fluency in English and Mandarin; strong communication and organizational skills.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Zoom
2mo
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Case Manager - Home Study and Post Release Services- Bilingual English/Spanish
Lincoln, Rhode Island, United States
OnsiteFull Time
2+ YOEBachelor’s in Human Services or related field; 2+ years case management in child/family services; bilingual English/Spanish; valid driver’s license; ability to pass background checks and TB test.
Microsoft Office Suite
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