236 study manager jobs at 110 companies in Abington, 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
1w
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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
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
3w
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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
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
3w
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Clinical Study Associate Manager
Armonk or Warren
$110k-$179k/yr HybridFull Time
4+ YOEBachelor's degree and 4+ years industry experience; clinical trial operations, ICH/GCP knowledge, vendor management, budget awareness, and strong communication skills required.
Microsoft Project, Microsoft PowerPoint, Microsoft Word, Microsoft Excel, CTMS, TMF, IVRS/IWRS, EDC
1w
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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)
1w
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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
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.
6d
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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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Clinical Trial Supply (CTS) Study Manager
King of Prussia or Marburg or Glattbrugg
HybridFull Time
5+ YOEBachelor's degree in life sciences, engineering, logistics, or equivalent experience; 5+ years in pharmaceutical clinical supply management; ICH-GCP, cGMP, and cGDP knowledge.
interactive response technology (IRT)
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
1mo
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Clinical Study Manager, Global 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, experience overseeing global trials and CRO/vendor management, knowledge of GCP/ICH, timeline/budget and risk management, study materials and site oversight; up to 10% travel.
EDC, eCOA
3d
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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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Clinical Trial Supply (CTS) Study Manager
Glattbrugg or King of Prussia or Marburg
HybridFull Time
5+ YOEBachelor's degree in life sciences, engineering, logistics, or equivalent experience; 5+ years in pharmaceutical clinical supply management; knowledge of ICH-GCP, cGMP, and cGDP.
Interactive Response Technology (IRT)
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
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