238 study manager jobs at 121 companies in Wyncote, PA
3mo
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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
2w
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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
4w
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Manager Clinical Study Lead
Armonk or Warren
$129k-$210k/yr HybridFull Time
6+ YOEBachelor's degree and 6+ years clinical research experience, strong budget and vendor management, knowledge of ICH/GCP, trial documentation, and leadership of cross-functional study teams.
CTMS, TMF, Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS, IWRS, EDC
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)
2w
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Study Director
South Brunswick Township or Dayton
$70k-$100k/yr OnsiteFull Time
5+ YOEBachelor's degree in a related field, 5+ years overseeing biocompatibility studies, knowledge of EPA, FDA, DOT, OECD, GLP, and ISO regulations, leadership, administration, communication, and writing skills.
EPA, FDA, DOT, OECD, GLP, ISO
1d
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Study Contracts Manager
Wilmington, Delaware, United States
$112k-$168k/yr HybridFull Time
4+ YOEBachelor's degree required, 4+ years negotiating clinical contracts and developing trial budgets, including Fair Market Value assessments. Requires ICH-GCP knowledge, communication, negotiation, analytical, and organizational skills.
TMF
2d
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Study Contracts Manager
Wilmington, Delaware, United States
$112k-$168k/yr OnsiteFull Time
4+ YOEBachelor’s degree required and 4+ years negotiating clinical contracts and developing trial budgets. Requires ICH-GCP knowledge, regulatory awareness, negotiation, communication, analytical, and organizational skills.
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
2w
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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
1mo
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Manager, Clinical Study Lead
Armonk or Warren
$129k-$210k/yr HybridFull Time
6+ YOEBachelor's degree with ≥6 years' industry experience; experience in global clinical trial operations, budget and vendor management; knowledge of ICH/GCP; proficiency with trial systems and Microsoft applications.
CTMS, TMF, Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, IVRS, IWRS, EDC
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
2d
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Federal Work Study
Philadelphia, Pennsylvania, United States
OnsitePart Time, Temporary
Currently enrolled university students with a high school diploma or GED. Requires professionalism, confidentiality, communication, time management, and ability to lift 25 pounds.
2mo
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Study Administrative Assistant
King of Prussia, Pennsylvania, United States
OnsiteFull Time
High school diploma or GED required; Excel and Word proficiency; strong organizational and documentation skills; ability to manage multiple tasks; on-site role in a laboratory environment.
Microsoft Excel, Microsoft Word
2w
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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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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)
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