169 trial manager jobs at 28 companies in Bunnlevel, NC
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Local Trial Manager (Sponsor Dedicated)
Durham, North Carolina, United States
$68k-$233k/yr OnsiteFull Time
2+ YOEBachelor's in life sciences,2+ years clinical research/project or trial management,knowledge of ICH GCP and local regulations,project financial awareness,MS Office proficiency,strong communication and problem solving.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
6d
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Senior Local Trial Manager (Sponsor Dedicated, Multiple Therapeutics)
Durham or Boston or Annapolis or Columbus or Bethlehem
$93k-$233k/yr RemoteFull Time
3+ YOEBA/BS in health or science preferred, 3–5+ years of trial management experience, complex clinical trial leadership, ICH-GCP and regulatory knowledge, strong IT skills, English and country-language proficiency, and occasional travel.
CTMS, eTMF/IF, CAPA
2mo
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Clinical Trial Manager
Durham or United States or Canada
$140k-$148k/yr RemoteFull Time
4+ YOE4+ years clinical research experience, university/college degree (life science preferred) or equivalent experience, knowledge of GCP/ICH, proficiency with Microsoft Office, EDC/CTMS/eTMF and vendor platforms; strong communication, planning, and financial awareness.
Microsoft Office, EDC, CTMS, eTMF, Veeva Vault, Medidata
2w
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Clinical Trial Manager - Full Service
Morrisville, North Carolina, United States
OnsiteFull Time
Lead site management, clinical and central monitoring, ensure GCP/regulatory compliance, manage CRA/CeM resources, develop clinical study tools, and mitigate trial risks.
Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards
2mo
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Clinical Trial Lead
Cary, North Carolina, United States
HybridFull Time
5+ YOEDegree in life sciences or nursing preferred; 5+ years clinical research; 1+ year as Senior CRA; knowledge of ICH GCP; oncology focus; CRO experience; strong English communication.
1d
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Senior Clinical Trial Manager (US)
Durham, North Carolina, United States
$112k-$222k/yr RemoteFull Time
2+ YOEBachelor's or equivalent in biological, physical, or health studies plus 4 years as a Senior CRA, or 2-year degree plus 6 years; 2 years CTM/LCRA experience, regulatory knowledge, passport, and driver's license.
FDA, ICH Guidelines
3w
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Business Development Manager - Clinical Trial Logistics (2260185)
Apex, North Carolina, United States
HybridFull Time
Proven new‑business sales experience in clinical trial or life‑sciences logistics, hunter mentality, CRM experience, bilingual English/Spanish, based near Raleigh NC, willingness to travel.
CRM
1mo
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Program Manager
Boston or Lexington or Austin or Nashville or Durham
$79k-$126k/yr HybridFull Time
Mass General Brigham: Provides integrated medical care, research, and clinical training services.
5+ YOEMasters required; 5+ years project management experience preferred in clinical research or multi-site trials. Experience with NIH-funded studies, federal regulations, trial operations, supervision of research staff, and monitoring enrollment/billing.
1w
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Senior Clinical Project Manager
Raleigh, North Carolina, United States
HybridFull Time
8+ YOELead planning and delivery of domestic/global late-phase clinical trials; 8+ years clinical trial/project management experience; bachelor’s in life sciences required (advanced degree preferred); strong CRO/vendor management and ICH-GCP knowledge.
2w
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Senior Project Manager
Raleigh, North Carolina, United States
RemoteFull Time
Experience managing international clinical trial projects in a CRO, knowledge of oncology/rare disease, vendor management, strong analytical and communication skills, bachelor’s degree in a science discipline.
6h
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Study Activation Manager
Raleigh, North Carolina, United States
HybridFull Time
8+ YOEBachelor's degree in science, healthcare, or related field or equivalent experience; 8 years of clinical research experience with significant study start-up, site activation, clinical operations, or trial management experience.
clinical trial management systems, start-up tracking tools, Microsoft Teams
4d
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QA Manager, GCP
Raleigh or United States
$112k-$153k/yr HybridFull Time
5+ YOEUniversity degree in life sciences or related discipline, 5+ years in pharmaceutical clinical quality assurance or clinical trials, GCP expertise, QA systems experience, and preferably auditing experience.
ICH GCP, FDA, EMA
1mo
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Site Network Manager (North America)
Raleigh or Austin or Tampa or San Francisco or New York City or Boston or Chicago or Nashville or Phoenix or Detroit or Minneapolis or Seattle or Las Vegas
$98k-$163k/yr RemoteFull Time
7+ YOE7+ years clinical research experience, bachelor’s degree required, site relationship management, knowledge of clinical trial lifecycle and ICH-GCP, strong communication and data-driven performance skills.
1mo
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Clinical Supply Chain Manager, Strategic Development
Research Triangle Park or Durham or California
HybridFull Time
3+ YOEManage clinical trial material manufacturing, forecasting, inventory, vendor oversight, labeling/distribution, and cross-functional coordination; IVRS/IWRS experience and knowledge of GCP/GMP required.
IVRS/IWRS, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
2w
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(Senior) Clinical Study Manager, Clinical Development
Research Triangle Park or Chicago
$110k-$160k/yr OnsiteFull Time
5+ YOE5+ years clinical trial management experience in biotech/pharma/CRO, Bachelor's in life sciences or nursing required; EDC/CTMS/eTMF proficiency, familiarity with SQL, oncology or molecular diagnostics experience.
EDC, CTMS, eTMF, SQL
4w
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Sr Manager, Statistical Programming
Foster City or Raleigh
$169k-$219k/yr HybridFull Time
2+ YOEAdvanced statistical programming leadership for clinical trials; BS/MS/PhD in Biostatistics or Computer Science plus relevant pharma/CRO experience; SAS, CDISC, regulatory submissions experience; strong communication and analytical skills.
SAS, SAS Macros, CDISC (CDASH, SDTM, ADaM)
3w
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Assoc Director, Statistical Programming
Foster City or Raleigh
$196k-$253k/yr HybridFull Time
8+ YOEAdvanced statistical programming experience for clinical trials, regulatory submissions, SAS and CDISC expertise, leadership and project management in pharma/CRO.
SAS, SAS Macros, Microsoft Excel, CDISC, ADaM, SDTM, CDASH
2w
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Counsel (Litigation)
Cary, North Carolina, United States
OnsiteFull Time
4+ YOE4+ years litigation experience; manage all aspects of litigation including e-discovery, discovery, motions, trials; manage outside counsel; familiarity with US litigation process; strong communication and prioritization skills.
1w
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Special Deputy Attorney General
Wake County, North Carolina, United States
$121k-$130k/yr OnsiteFull Time
5+ YOELicensed to practice law in North Carolina, five+ years progressive litigation experience, trial advocacy, written/oral advocacy, ability to manage complex eminent domain cases and special projects.
1mo
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Clinical Research Coordinator I
Raleigh, North Carolina, United States
OnsiteTemporary
1+ YOEConduct and manage clinical trials per protocol and GCP; regulatory document preparation, subject recruitment, data entry, adverse event reporting, phlebotomy and clinical task performance as required.
Microsoft Office
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