1mo
Save
Mark Applied
Hide
Study Manager
Chandler or Tucson
OnsiteFull Time
10+ YOE10+ years study/project management experience in mining or heavy industry; bachelor\u0002s in engineering preferred; PE preferred; strong leadership, risk/value management, communication, and stakeholder liaison skills.
1mo
Save
Mark Applied
Hide
Study Manager
Chandler, Arizona, United States
HybridFull Time
10+ YOE6+ MgmtLeads mining studies with 10+ years PM experience; strong leadership, risk management, stakeholder liaison; Bachelor's in Engineering; PE license preferred; MBA asset.
Project management software
1mo
Save
Mark Applied
Hide
Clinical Study Manager
Fridley, Minnesota, United States
$110k-$160k/yr OnsiteFull Time
5+ YOELead clinical study execution and operations, site management, and data/regulatory compliance.
EDC systems, CTMS platforms, Clinical trial tracking tools
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
Study Manager - Oncology
Morrisville, North Carolina, United States
OnsiteFull Time
Bachelor’s in life sciences or related field; CRO/pharma experience; strong GCP knowledge; excellent organizational and communication skills; travel ~25%; experience in oncology/clinical studies preferred.
3w
Save
Mark Applied
Hide
Study Manager
Miami, Florida, United States
$85k-$95k/yr OnsiteFull Time
2+ YOEMinimum 2 years clinical research coordination/project management; knowledge of FDA regulations and ICH/GCP; strong planning, communication, team leadership, TMF and study documentation oversight.
TMF
2mo
Save
Mark Applied
Hide
Sr. Study Manager, Clinical Operations
Princeton, New Jersey, United States
$167k-$196k/yr HybridFull Time
3+ YOELead global oncology clinical studies; manage timelines, budgets, CROs; strong leadership in Clinical Operations.
CTMS, TMF, eCRF, IRT, Central Lab, CRO management
2mo
Save
Mark Applied
Hide
Study Manager (Canada or United-States)
Montreal or Toronto or Vancouver or Salt Lake City
$150k-$200k/yr HybridFull Time
10+ YOE3+ MgmtLead multi-disciplinary studies for mining projects; 10+ years EPC/EPCM or design & construction; PE licensed or eligible; PEA/PFS/FS experience; client and supplier management.
MS Project, Primavera P6
2mo
Save
Mark Applied
Hide
Sr. Study Manager, Clinical Operations
Princeton, New Jersey, United States
$167k-$196k/yr HybridFull Time
3+ YOELead global clinical studies; manage timelines and budgets; coordinate CROs/vendors; collaborate across cross-functional teams; ensure compliance.
2mo
Save
Mark Applied
Hide
Study Manager - Immunology
United States
RemoteFull Time
Bachelor’s degree in life sciences; CRO experience preferred; strong knowledge of GCP and regulatory requirements; excellent organizational, communication, and leadership skills; willingness to travel ~25%.
GCP, SOPs, TMF systems, Project management software, Microsoft Excel, PowerPoint
1mo
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
2w
Save
Mark Applied
Hide
Clinical Study Manager
Rochester, New York, United States
$100k-$150k/yr RemoteFull Time
Bachelor's degree or equivalent, experience in clinical operations/drug-device development, ophthalmology experience preferred, knowledge of FDA/ICH/GCP/HIPAA/IRB, project management skills, strong communication and analytical abilities, Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft Teams, SurveyMonkey, Microsoft Forms, EDC, eCRF
1mo
Save
Mark Applied
Hide
Study Project Manager II
Irvine, California, United States
$125k-$237k/yr HybridFull Time
8+ YOEBachelor's degree required; 8+ years clinical research study management; leadership and cross-functional experience; experience with drug/device/interventional studies and end-to-end study operations; familiar with ICH/GCP and clinical trial systems (EDC, IRT, CTMS, eTMF).
EDC, IRT, CTMS, eTMF
1mo
Save
Mark Applied
Hide
Clinical Study Manager
Plano, Texas, United States
OnsiteFull Time
3+ YOEBachelor’s in Life Sciences, Engineering, or related field; 3–8+ years clinical research; 2+ years medical device study management; ISO14155/FDA/GCP knowledge; EDC/CTMS/eTMF proficiency.
EDC, CTMS, eTMF
2mo
Save
Mark Applied
Hide
Study Director I
Salt Lake City, Utah, United States
OnsiteFull Time
Direct scientific studies, ensure regulatory compliance, manage study timelines, and report results.
Microsoft Office, LIMS
1w
Save
Mark Applied
Hide
Study Manager I (3910)
Brookline, Massachusetts, United States
$80k-$105k/yr OnsiteFull Time
5+ YOEEnsures regulatory-compliant clinical trial conduct at assigned sites, maintains study documentation, trains site staff, enforces safety reporting, and supports enrollment and data quality.
EDC, IVRS
1w
Save
Mark Applied
Hide
Manager Study Start-up
Aliso Viejo or San Clemente or Burlington or United States
$130k-$163k/yr OnsiteFull Time
8+ YOE8+ years clinical research experience in medical device/pharma; experience leading study execution, timelines, budgets, and cross-functional teams; strong knowledge of FDA regulations and GCP; risk management skills.
1mo
Save
Mark Applied
Hide
Study Start-Up Project Manager
Cincinnati, Ohio, United States
OnsiteFull Time
5+ YOEBachelor's required (advanced degree preferred),5+ years clinical research experience, project management and leadership in study start-up, cardiovascular/metabolic experience desired, strong communication skills.
3w
Save
Mark Applied
Hide
Clinical Study Operations Engineering Program Manager - Health
Sunnyvale, California, United States
OnsiteFull Time
Experience managing clinical study operations, CRO onboarding, recruitment strategy, analytics-driven insights, and international expansion for study recruitment.
3mo
Save
Mark Applied
Hide
Study Start-Up Project Manager
Denver or Cincinnati
$100k-$165k/yr OnsiteFull Time
5+ YOEBachelor's required (advanced degree in life sciences preferred), 5+ years clinical research experience in study start-up (senior/lead role at a CRO preferred), project management and leadership experience, strong oral/written communication.
Explore Jobs