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Clinical Trial Manager/Senior Clinical Trial Manager
Waltham or Menlo Park
$146k-$187k/yr HybridFull Time
5+ YOELead clinical trials, manage budgets and vendors, ensure regulatory compliance; 5-7+ years in clinical operations; GCP knowledge.
3mo
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Clinical Trial Manager
Cambridge, Massachusetts, United States
$140k-$168k/yr OnsiteFull Time
5+ YOE5+ years in clinical trial operations with cross-functional leadership; strong GMP/ICH knowledge; budget and risk management.
MS Project, MS Word, MS Excel, PowerPoint
2mo
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Clinical Trial Manager
Watertown, Massachusetts, United States
$115k-$200k/yr OnsiteFull Time
3+ YOEBachelor of Science in Life Sciences; 3+ years as a CTM or 5+ years as a Sr. CTM; experience on large global Phase 2 trials; strong PM, regulatory knowledge, and communication skills.
CTMS, EDC, eCRF, GCP, Clinical data management
1mo
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Senior Clinical Trial Manager (Global)
Boston, Massachusetts, United States
$179k-$211k/yr HybridFull Time
5+ YOEBachelor's in life sciences required, 5+ years clinical trial management experience in pharma/biotech/CRO, global trial and CRO/vendor oversight experience, Phase 2/3 and oncology preferred, strong project management and communication skills.
4d
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Senior Clinical Trial Manager
Waltham, Massachusetts, United States
$143k-$175k/yr HybridFull Time
8+ YOE8+ years clinical trial experience managing CROs and vendors, deep GCP/ICH knowledge, strong organizational and communication skills, ability to lead cross-functional teams and travel as needed.
Microsoft Office Suite, MS Project, Smartsheet
2mo
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Senior Clinical Trial Manager
Cambridge, Massachusetts, United States
OnsiteFull Time
5+ YOELead clinical operations for trials, manage CROs and sites, ensure on-time, on-budget delivery and regulatory compliance.
GCP, ICH, FDA regulations
3mo
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Sr. Clinical Trial Manager
Cambridge, Massachusetts, United States
$164k-$185k/yr OnsiteFull Time
6+ YOEMinimum 6 years in clinical trial management in biotech/pharma; strong vendor/CRO management; knowledge of GCP/ICH regulatory requirements; strong PM skills; travel up to 15%.
2w
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Senior Clinical Trial Manager
Boston, Massachusetts, United States
$180k-$205k/yr RemoteFull Time
7+ YOEBA/BS and 7+ years managing clinical trial activities, strong ICH/GCP knowledge, global trial and CRO/vendor oversight experience, excellent communication, and willingness to travel ~20%.
eCRF, EDC, PROs
1mo
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Sr./Clinical Trial Manager – Clinical Operations
Boston, Massachusetts, United States
$123k-$176k/yr OnsiteFull Time
3+ YOEB.S. or equivalent; 3+ years clinical trial management experience (5+ if senior); oncology experience required; knowledge of ICH GCP; CRO/vendor oversight; ability to manage global teams; willingness to travel 10-20%.
3mo
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Sr. Manager - Clinical Trial Lead
Cambridge or Research Triangle Park
$141k-$188k/yr HybridFull Time
6+ YOE6+ Mgmt6+ years in clinical operations management; outsourced trials; strong GCP/ICH knowledge; budgeting; CRO management.
Planisware, Veeva CTMS, Beacon
1mo
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(Sr.) Clinical Trial Manager
Cambridge, Massachusetts, United States
$165k-$190k/yr OnsiteFull Time
4+ YOEBA/BS in Health or Life Sciences required; minimum 4+ years clinical trials management experience; strong communication, organizational and project leadership skills; CRO/vendor management and ability to travel required.
eTMF, ICH/GCP
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.
3d
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Principal Clinical Trial Manager
Andover, Massachusetts, United States
$137k-$194k/yr OnsiteFull Time
8+ YOEBA/BS in science or life sciences,8+ years clinical trial experience in pharma/biotech/CRO (8-10 preferred),experience with IRB/EC submissions,GCP/ICH/FDA knowledge,EDC experience,clinical budget and vendor management.
Electronic data capture (EDC)
3mo
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Senior Clinical Trial Manager
Boston, Massachusetts, United States
$140k-$175k/yr HybridFull Time
5+ YOE5+ years in clinical operations for FDA-regulated devices or digital health; proven site management and IRB/submission experience; strong data management and cross-functional coordination.
1mo
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Clinical Trial Marketing Manager (US)
Haverhill, Massachusetts, United States
HybridFull Time
5+ YOE5+ years marketing experience in clinical trial services/healthcare consulting or strategic marketing; strong knowledge of clinical trial processes (ideally respiratory); proven strategy-to-execution experience, stakeholder influence, and excellent communication skills.
3mo
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Senior Clinical Trial Associate
San Francisco or Cambridge
$110k-$120k/yr HybridFull Time
3+ YOEBachelor's degree required; minimum 3 years in clinical trials; FDA/EMA/ICH/GCP familiarity preferred; strong MS Office; vendor and site coordination; TMF and study documentation management.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
1w
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Associate Director, Global Clinical Trial Manager
Billerica, Massachusetts, United States
$145k-$200k/yr HybridFull Time
8+ YOEBachelor's in life sciences or related,8+ years drug development,5+ years clinical development/project management in pharma/CRO,PMP preferred,master's preferred,familiarity with protocols/CSRs/IBs,strong communication and cross‑functional leadership.
2w
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Sr. Clinical Trial Associate
Waltham, Massachusetts, United States
$115k-$159k/yr OnsiteFull Time
Deciphera Pharmaceuticals: Developing targeted kinase inhibitors for the treatment of cancer.
3+ YOEBachelor's or Master's degree and at least 3 years clinical operations experience in pharma or CRO; solid understanding of ICH/GCP and regulatory requirements; ability to manage trial components independently with strong attention to detail.
Trial Master File (TMF)
1mo
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Clinical Trial Manager (CTM or Sr. CTM)
Watertown, Massachusetts, United States
$135k-$180k/yr OnsiteFull Time
3+ YOEBachelor's in a scientific/health discipline, 3+ years clinical operations/CTM experience (CRO/biotech/pharma) preferably in oncology, leadership and cross-functional experience, contract and budget management, GCP/ICH compliance, Microsoft Project/Word/PowerPoint/Excel.
Microsoft Project, Microsoft Word, Microsoft PowerPoint, Microsoft Excel
1mo
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Associate Director, Trial Lead Clinical Operations (Contract to Perm)
Bedford, Massachusetts, United States
OnsiteFull Time, Contract
5+ YOELead global clinical trial operations with 5+ years' clinical trial experience, GCP/FDA knowledge, protocol and TMF oversight, CRO/vendor management, and up to 25% travel.
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