251 study manager jobs at 121 companies in Yardley, PA
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.
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
2d
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Manager Study Start Up
Princeton, New Jersey, United States
$139k-$163k/yr OnsiteFull Time
5+ YOE5+ years experience in feasibility and study start-up, site agreements, budget negotiation, ICH/GCP knowledge, strong communication, financial acumen, and proficiency with MS Office and eTMF.
Microsoft Word, Microsoft Excel, eTMF, grant plan
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.
3w
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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
4w
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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
1w
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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, vendor management, trial operations, budget awareness, and proficiency with IVRS/IWRS, EDC, TMF and MS Office.
Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS/IWRS, EDC, TMF
1d
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Study Manager I (4078)
Philadelphia, Pennsylvania, United States
OnsiteFull Time
5+ YOEHigh school diploma required; bachelor's degree and ACRP certification preferred. Requires 5+ years of clinical research experience, strong communication, English proficiency, and clinical trial regulatory knowledge.
Electronic Data Capture (EDC), Interactive Voice Response System (IVRS)
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
3w
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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
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.
3d
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Executive Director, Program and Study Management, Immunology and Neurosciences
Rahway or Upper Gwynedd
$256k-$403k/yr HybridFull Time
12+ YOEBachelor's required; advanced scientific degree preferred. 12+ years clinical development experience; deep GCP/ICH knowledge, digital/AI leadership, program/study delivery and people development experience.
Artificial Intelligence (AI), eTMF
2w
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Senior Medical Study Leader- Vaccines
Morristown, New Jersey, United States
$149k-$215k/yr OnsiteFull Time
8+ YOEAdvanced degree in life sciences,8+ years clinical research/project management experience,knowledge of GCP/GEP/GPP,experience in multi-country trials and real-world evidence,project management certification preferred.
1mo
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Home Study Case Worker - Per Diem (4863)
East Orange, New Jersey, United States
$32-$35/hr FieldPart Time, Temporary
BSW or equivalent degree required, experience conducting home studies and child welfare/case management preferred, bilingual English/Spanish, strong writing and interpersonal skills, ability to travel up to 80% with limited notice.
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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Study Responsible Physician- Neuroscience Late Development
Titusville or Spring House or Switzerland
$199k-$344k/yr HybridFull Time
1+ YOEMD (or equivalent) required; 1+ year clinical trials experience in pharma/biotech/CRO (or 2 years in academia); neuroscience experience preferred; GCP knowledge; medical monitoring, protocol development, safety review skills; Microsoft Excel/Word proficiency.
Microsoft Excel, Microsoft Word
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.
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