181 study manager jobs at 95 companies in West Chester, PA
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
1mo
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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
1w
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Participant Recruitment & Study Startup Manager
Chadds Ford or San Jose or Boston or Cambridge
OnsiteFull Time
Experience in participant recruitment, human factors, clinical or market research, study coordination, or related work; project management, communication, organization, problem-solving, and recruitment strategy skills required.
CRM, participant databases, scheduling platforms, research management software
3mo
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Study Coordinator
Newark, Delaware, United States
HybridFull Time
3+ YOEPh.D. with 3 years or M.S. with 10 years in toxicology/animal sciences; GLP rodent study experience, people management, hands-on DART techniques, GLP documentation, Instem Provantis and Microsoft Office skills.
Microsoft Office, Instem Provantis
2w
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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
1mo
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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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Global Study Lead
United States or Philadelphia or Cambridge
$145k-$196k/yr HybridFull Time
7+ YOE3+ MgmtRequires a bachelor's degree, 7+ years of clinical research experience, 3–5 years leading global trials, Phase 3 experience, CRO oversight, leadership, project management, and MS Office/MS Project proficiency.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Project
1w
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Global Study Lead
Cambridge or Philadelphia
$145k-$196k/yr HybridFull Time
7+ YOE3+ MgmtBachelor's degree, 7+ years of clinical research experience, and 3–5 years leading global Phase 1–4 trials including Phase 3 registrational studies. Requires CRO oversight, leadership, project management, and Microsoft Office and Project proficiency.
Microsoft Office Suite, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Project
3mo
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Study Coordinator
Newark, Delaware, United States
OnsiteFull Time
3+ YOEPhD with 3+ years or MS with 10+ years in toxicology/animal sciences; leads team; GLP experience; strong communication.
MS Office, Instem Provantis
3mo
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Study Coordinator
Newark, Delaware, United States
OnsiteFull Time
3+ YOEPh.D. with 3+ years or M.S. with 10+ years in toxicology/animal sciences; GLP rodent toxicity experience; leadership of technical staff; strong communication and documentation skills.
MS Office, Instem Provantis
1w
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Local Study Associate Director
Wilmington, Delaware, United States
$138k-$207k/yr HybridFull Time
3+ YOEBachelor's degree in a related field preferred, 3+ years in development operations or related clinical research, ICH-GCP and regulatory knowledge, project leadership, communication, organization, negotiation, and travel ability.
CTMS, eTMF
1w
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Child Study Team Case Manager
Mickleton, New Jersey, United States
$63k-$94k/yr OnsiteFull Time
Requires a valid New Jersey Educational Services Certificate with School Social Worker or School Psychologist certification, special education knowledge, communication skills, and background screening.
personal computers, printer, copy machine, fax machine, telephone
2w
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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
1w
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Local Study Associate Director
Wilmington, Delaware, United States
$138k-$207k/yr HybridFull Time
3+ YOEBachelor's degree in a related field and 3+ years in development operations or related clinical research. Requires ICH-GCP and regulatory knowledge, clinical trial leadership, project management, communication, organization, negotiation, and travel ability.
CTMS, eTMF
5d
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NIS P&D Study Delivery Lead, Associate Director
Stevenage or Upper Providence or Cambridge
HybridFull Time
Bachelor's degree in life sciences or related field, clinical operations or research experience, regulatory knowledge, budgeting skills, and leadership of cross-functional teams; advanced degree and NIS experience preferred.
Good Clinical Practice (GCP)
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
2mo
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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.
1d
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Clinical Research Study Lead - Developmental and Behavioral Pediatrics
Philadelphia, Pennsylvania, United States
$69k-$88k/yr OnsiteFull Time, Part Time
2+ YOEBachelor's degree and at least 2 years of complex research experience required. Requires GCP knowledge, clinical research, regulatory compliance, communication, organization, project management, and analytical skills.
FDA, Institutional Review Board (IRB), CTSA, NIH, HIPAA, 21 CFR
1w
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Head, Program and Study Management Oncology
Rahway or North Wales
$311k-$489k/yr HybridFull Time
12+ YOEBachelor's degree and 12+ years in pharmaceutical, biotechnology, or CRO clinical operations required; leadership of clinical programs, AI-enabled modernization, budgets, vendors, GCP/ICH, and global teams.
AI, predictive analytics, automation
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