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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.
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.
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
1mo
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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
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.
1w
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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.
1w
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Head, Program and Study Management Oncology
Rahway or North Wales
$311k-$489k/yr HybridFull Time
12+ YOESenior clinical operations leader with 12+ years in pharma/biotech/CRO, accountable for end-to-end program delivery; bachelor's required, advanced degree preferred; expertise in GCP/ICH, vendor management, and digital/AI-enabled solutions.
eTMF
1mo
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AY 26-27 Study Abroad Assistants-Center for Global Engagement
Ewing Township, New Jersey, United States
$16/hr OnsitePart Time
Comfortable speaking to small groups, proficiency with Google Workspace and Canva, ability to learn application management software (e.g., Terra Dotta), meticulous with paperwork and deadlines; preferred study abroad experience.
Google Workspace, Canva, Terra Dotta
1mo
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Executive Director, Study Support & Oversight
Malvern or San Diego or United States
HybridFull Time
12+ YOE5+ MgmtBachelor's degree required; 12+ years clinical operations experience with 5+ years leadership; experience overseeing CROs/vendors, Phase 1–3 trials, ICH-GCP/FDA regulations, inspection readiness, and strong operational leadership.
3w
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Anticipated, Supervisor of Child Study Teams (26 - 27 School Year) - DIST
Somerset, New Jersey, United States
$100k/yr OnsiteFull Time
NJ administrative certification, Master’s degree, valid NJ school psychologist/social worker/LDT-C certification, multi-year Child Study Team experience, successful evaluations, criminal history clearance, and proof of work authorization.
Google Suite, IEP software program, Genesis Employee Portal, Student Information System
2w
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Program Manager (Preclinical)
Princeton or Los Angeles
$80k-$120k/yr HybridFull Time
Bachelors or Masters in life/chemical sciences, contract management and study coordination experience in pharma/biotech, strong organization and communication, proficiency with Microsoft Word/Excel/PowerPoint/Outlook.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
1mo
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Assistant Project Manager
Philadelphia or Cleveland or Columbus or Detroit
$80k-$105k/yr OnsiteFull Time
Several years of project management/accounting experience in construction preferred; AS/BS preferred in business/accounting/finance/legal studies/construction management; proficient in Microsoft Office (Excel & Word); strong communication and accounting knowledge.
Microsoft Office, Microsoft Excel, Microsoft Word
2mo
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Assistant Project Manager - Environmental Siting & Routing (Conshohocken, PA)
Conshohocken, Pennsylvania, United States
OnsiteFull Time
5+ YOEAssist with managing environmental projects, routing studies, NEPA analysis, and permitting; lead tasks; develop proposals; manage client relationships.
3w
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Senior Manager, Clinical Trial Business Delivery
Princeton, New Jersey, United States
$135k-$164k/yr OnsiteFull Time
Oversee clinical study operations, manage CROs/vendors, ensure compliance with regulations and SOPs, monitor trial progress and risks, support audits and CAPAs.
1w
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Senior Project Manager Clinical Research
Princeton, New Jersey, United States
$87k-$173k/yr OnsiteFull Time
10+ YOEBachelor's degree and 10+ years clinical research/medical affairs/project management experience; knowledge of clinical trials, study oversight, budgeting, statistics, strong communication and leadership; travel up to 10-15%.
3w
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Senior Manager, Clinical Trial Business Delivery
Princeton, New Jersey, United States
$135k-$164k/yr OnsiteFull Time
Oversee clinical trial operations, manage risks and CRO/vendor relationships, ensure regulatory and SOP compliance, support audits/inspections and CAPA resolution, and monitor study progress.
1mo
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Assistant Director of Financial Aid/ Work Study Coordinator
Malvern, Pennsylvania, United States
OnsiteFull Time
Familiarity with federal, state, and institutional financial aid regulations; experience processing financial aid (file review, needs analysis, packaging, federal verification); administration and oversight of Federal Work-Study and student employment programs.
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