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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.
1mo
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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.
3d
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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 Manager I (3769)
Philadelphia, Pennsylvania, United States
OnsiteFull Time
5+ YOEEnsure protocol and regulatory compliance (FDA, ICH-GCP), complete required trainings (ICH-GCP, IATA), maintain site documentation, manage clinical trial conduct and enrollment; minimum 5 years clinical research experience; HS required, bachelor’s preferred; ACRP preferred; strong communication skills.
EDC, IVRS
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
3d
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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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Study Optimization Manager-1
Collegeville or Wavre or Ware RD or Zebulon
€80k-€134k/yr OnsiteFull Time
Bachelor's in a relevant STEM or supply-chain field (or equivalent experience); strong knowledge of clinical supply, CMC, forecasting, data integration and advanced demand modelling; experience compiling and analyzing multi-source data and communicating model outputs.
N-Side Supply Application, Intel Hub, IRT, fusion, Continuous Integration / Continuous Delivery
1d
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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.
2w
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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.
1w
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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
2d
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Senior Program Manager - Medical & Clinical Affairs
Bridgewater or Chicago or Washington or Boston or Atlanta or Orlando or Philadelphia or Lexington
RemoteFull Time
7+ YOEBachelor's in engineering or science preferred,7+ years managing technical projects in medical device/pharma,project management qualification preferred (PMP/APM),clinical study execution experience,strong communication and stakeholder management.
Microsoft Word, Microsoft Project, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams, database software, SAP, Microsoft Outlook, Project Management Cloud Software
4w
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Project Manager II
Whitehall or Pennsylvania or Maryland or New York or New Jersey or District of Columbia
FieldFull Time
2+ YOERequires 3 years of undergraduate studies in chemical engineering or related field, 2 years experience with stack testing and air emissions testing, QSTI certification (Group 1), knowledge of EPA/OSHA regulations and testing methods, ability to manage field projects and mentor staff.
1mo
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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.
3d
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Staff Assistant - Study Hall
Emmaus, Pennsylvania, United States
OnsitePart Time
High school diploma/GED, CPR and basic first aid, ability to supervise and manage students, basic clerical and computer skills, reliable attendance and ability to travel to assigned locations.
3w
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NJ School Psychologist (Child Study Team)
Camden, New Jersey, United States
$94k-$113k/yr OnsiteFull Time
3+ YOEMaster's in School Psychology (or higher) and NJ School Psychologist certification required; 3+ years preferred; experience with psychoeducational evaluations, IEP development, case management, counseling, and working with multilingual learners.
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