259 study manager jobs at 120 companies in Trenton, NJ
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
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
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.
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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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
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
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
1w
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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
2mo
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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.
1d
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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
2w
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Clinical Study Data Lead - East Hanover
East Hanover, New Jersey, United States
$120k-$222k/yr HybridFull Time
5+ YOEBachelor's in life sciences/computer science or equivalent; 5+ years clinical data management experience; strong GCP, data standards, regulatory knowledge; leadership and cross-functional influence skills.
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