381 study manager jobs at 189 companies in Princeton, NJ
2mo
Save
Mark Applied
Hide
Study Manager
New York City, New York, United States
OnsiteFull Time
5+ YOE5–7 years coordinating multi-site clinical studies; IRB submissions; site management; ICH-GCP; HIPAA; FDA knowledge; strong organization.
EDC, IRB platforms, eTMF, protocols, spreadsheets, data management
2mo
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
Senior Global Clinical Study Manager
Chicago or Dallas or Durham or Gilbert or Indianapolis or New York or Phoenix or Rockville or San Francisco or Tampa
$93k-$233k/yr RemoteFull Time
5+ YOE2+ MgmtBachelor's in life sciences,5+ years clinical research experience including 2+ years clinical study management; oncology and global trial experience; knowledge of ICH-GCP, regulatory requirements, financial management.
Microsoft Office, CTMS, EDC
1w
Save
Mark Applied
Hide
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
1w
Save
Mark Applied
Hide
Clinical Study Operations Manager
Boston or New York City or Paris
$90k-$110k/yr RemoteFull Time
Experience in clinical project/operations, strong project management and communication, familiarity with GCP/ICH and decentralized data collection, attention to detail, ability to manage multiple priorities.
Zendesk, Asana
4w
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
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
2mo
Save
Mark Applied
Hide
Director, Clinical Study Management
Jersey City or Millbrae
$203k-$221k/yr HybridAll Commitments Available
12+ YOE12+ years in clinical study management; oncology focus; leadership in matrix org; strong GCP/ICh knowledge.
1mo
Save
Mark Applied
Hide
Senior Global Clinical Study Manager
Durham or Phoenix or Gilbert or San Francisco or New York City or Indianapolis or Tampa or Rockville or Chicago or Dallas
$93k-$233k/yr OnsiteFull Time
5+ YOE2+ MgmtBachelor's in life sciences, 5+ years clinical research/monitoring (including 2 years study management), Phase III and oncology experience, ICH-GCP and FDA knowledge, global trial and financial management, stakeholder leadership.
Microsoft Office, CTMS, EDC
1w
Save
Mark Applied
Hide
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)
6d
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
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
3mo
Save
Mark Applied
Hide
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
1w
Save
Mark Applied
Hide
Study Manager I, Extractable and Leachable
Fairfield, New Jersey, United States
$65k-$90k/yr OnsiteFull Time
2+ YOEBachelor's in chemistry, 2 years E&L project experience with protocol/report writing, knowledge of HPLC/MS, GC/MS or ICP/MS, GMP familiarity, project management and strong communication skills.
HPLC/MS, GC/MS, ICP/MS, MS Office
4w
Save
Mark Applied
Hide
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.
5d
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
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)
6d
Save
Mark Applied
Hide
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
3w
Save
Mark Applied
Hide
Senior Study Management Specialist
Boston or New York City
$95k-$105k/yr HybridFull Time
2+ YOEMinimum 2 years study management/clinical trial coordination experience in US clinical research; degree in a scientific discipline; strong written communication, attention to detail, and knowledge of RWE and regulatory requirements.
1w
Save
Mark Applied
Hide
Manager, Independent Study Program (ISP)
New York City, New York, United States
$70k-$75k/yr OnsiteFull Time
3+ YOEBA or BFA required; MA or MFA preferred. Requires 3–5 years of related academic or museum experience, strong organization and communication, budget management, judgment, initiative, and professionalism.
Explore Jobs