2mo
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Study Manager
New York City, New York, United States
OnsiteFull Time
5+ YOE5–7 years coordinating multi-site clinical studies; IRB submissions; site management; ICH-GCP; HIPAA; FDA knowledge; strong organization.
EDC, IRB platforms, eTMF, protocols, spreadsheets, data management
2mo
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Sr. Study Manager, Clinical Operations
Princeton, New Jersey, United States
$167k-$196k/yr HybridFull Time
3+ YOELead global oncology clinical studies; manage timelines, budgets, CROs; strong leadership in Clinical Operations.
CTMS, TMF, eCRF, IRT, Central Lab, CRO management
2mo
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Sr. Study Manager, Clinical Operations
Princeton, New Jersey, United States
$167k-$196k/yr HybridFull Time
3+ YOELead global clinical studies; manage timelines and budgets; coordinate CROs/vendors; collaborate across cross-functional teams; ensure compliance.
4d
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Study Manager, Clinical Operations
North Wales or Rahway or San Diego
$96k-$151k/yr OnsiteFull Time
2+ YOEBachelor's degree plus 2 years (or Master's plus 1 year) in pharmaceutical/clinical development or project management, knowledge of GCP/ICH, project planning, stakeholder management, and Microsoft Office.
Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Microsoft Outlook, Microsoft Office
2mo
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Clinical Research Study Manager
Philadelphia, Pennsylvania, United States
OnsiteFull Time
5+ YOELeading clinical studies, ensuring protocol compliance, site training, data quality, and enrollment goals.
EDC, IVRS, IATA, ICH-GCP knowledge, ALCOA-C
2mo
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Sr. Study Manager, Clinical Operations
Princeton, New Jersey, United States
$167k-$196k/yr HybridFull Time
3+ YOE3-5 years clinical trial management; strong communication; global study leadership; familiarity with FDA/GCP/ICH; Bachelor's in biological sciences.
1d
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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
2w
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Associate Global Study Manager
Conshohocken, Pennsylvania, United States
OnsiteFull Time
1+ YOEBachelor's preferred,1–3 years post-graduate experience,proficiency with Microsoft 365 and reporting tools,strong written/oral communication,attention to detail,and ability to handle sensitive data.
Microsoft 365
3w
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Clinical Study Associate Manager
Armonk or Warren
$110k-$179k/yr HybridFull Time
4+ YOEBachelor's degree and 4+ years clinical trial experience, knowledge of ICH/GCP, trial operations, vendor management, budget awareness, and strong communication and data skills.
Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS/IWRS, EDC, TMF
2mo
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Director, Clinical Study Management
Jersey City or Millbrae
$203k-$221k/yr HybridAll Commitments Available
12+ YOE12+ years in clinical study management; oncology focus; leadership in matrix org; strong GCP/ICh knowledge.
1mo
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Senior Global Clinical Study Manager
Durham or Phoenix or Gilbert or San Francisco or New York City or Indianapolis or Tampa or Rockville or Chicago or Dallas
$93k-$233k/yr OnsiteFull Time
5+ YOE2+ MgmtBachelor's in life sciences, 5+ years clinical research/monitoring (including 2 years study management), Phase III and oncology experience, ICH-GCP and FDA knowledge, global trial and financial management, stakeholder leadership.
Microsoft Office, CTMS, EDC
2mo
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Study Coordinator
King of Prussia, Pennsylvania, United States
OnsiteFull Time
2+ YOEAssociate or Bachelor’s degree in a scientific/administrative/technical field; 2–4 years in research or lab; regulatory knowledge; strong communication; Smartsheet and MS Office; experience in CRO/preclinical settings.
Smartsheet, Microsoft Office, NetSuite, Electronic Data Management
2mo
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Senior Study Startup Specialist
Princeton, New Jersey, United States
$90k-$115k/yr HybridFull Time
5+ YOEBachelor's degree; 5-8 years in clinical study start-up/regulatory submissions; oncology trials; CTMS/eTMF proficiency; strong negotiation and leadership.
CTMS, eTMF, clinical trial platforms
2d
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Study Manager I, Extractable and Leachable
Fairfield, New Jersey, United States
$65k-$90k/yr OnsiteFull Time
2+ YOEBachelor's in chemistry, 2 years E&L project experience with protocol/report writing, knowledge of HPLC/MS, GC/MS or ICP/MS, GMP familiarity, project management and strong communication skills.
HPLC/MS, GC/MS, ICP/MS, MS Office
2w
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Associate Director, Study Toxicologist
Conshohocken, Pennsylvania, United States
$178k-$218k/yr OnsiteFull Time
10+ YOEPhD in toxicology/pharmacology/DMPK,10+ years pharmaceutical/biotech nonclinical development experience, CRO study management, protocol/report review, strong communication and multitasking skills.
1mo
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Clinical Study Manager, Clinical Operations (Basking Ridge, NJ, US, 07920)
Basking Ridge, New Jersey, United States
$136k-$204k/yr OnsiteFull Time
3+ YOEBSc required, 3+ years clinical trial experience with global study oversight, CRO/vendor management, GCP/ICH compliance, risk and timeline management, and ability to travel up to 10%.
eCOA, EDC
1w
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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 Delivery Lead
Short Hills, New Jersey, United States
RemoteFull Time
10+ YOE10+ years clinical trial delivery experience with strong operational, regulatory (GCP/GDPR), analytical and financial literacy; proven program delivery, project-management methodology design, and client-facing leadership; CRIO, HubSpot, Monday.com experience.
CRIO, HubSpot, Monday.com
2w
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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.
3w
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Research Study Assistant
New York City, New York, United States
$57k-$58k/yr OnsiteFull Time
Bachelor's degree or equivalent, customer-service orientation, strong Excel and Microsoft Office skills, ability to learn systems, work semi-independently and manage multiple tasks.
Microsoft Office, Microsoft Excel, REDCap, Qualtrics, Electronic Medical Records (EMR)
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