8 trial manager jobs at 6 companies in Xenia, OH
3mo
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Experienced Clinical Trial Project Manager
Cincinnati, Ohio, United States
OnsiteFull Time
5+ YOEBachelor's degree and 5+ years managing clinical trials; broad knowledge of medical terminology and clinical research methodology.
3mo
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Clinical Trial Project Manager
Cincinnati, Ohio, United States
OnsiteFull Time
1+ YOEBachelor’s Degree and 1-3 year of research-related experience; broad knowledge of medical terminology and clinical research methodology.
1mo
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Trial Technician Lead
Hillsboro, Ohio, United States
OnsiteFull Time
1+ YOEAssociate degree, 1–2 years relevant experience, Microsoft Office proficiency, strong communication, math, time-management, attention to detail, and ability to multitask.
Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Microsoft Outlook, PC, scanner
2w
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PhD & Postdoctoral Virtual Career Event: Associate Clinical Trial Manager - Cardio, Renal, GI, Metabolic - September 10
Cincinnati, Ohio, United States
OnsiteFull Time
PhD in life sciences required; background in cardiovascular, renal, GI, endocrine, or metabolic; English fluency and presentation skills; ability to work in a fast-paced industry.
Microsoft Teams
4w
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Technology Product Development Specialist
Marysville, Ohio, United States
OnsiteFull Time
5+ YOEBachelor's in food science/technology required (Master preferred), minimum 5 years in food & beverage, experience with formulation and trial management, project management skills, and consumer insight understanding.
NesTMS, Nestle Idea to Launch (I2L)
3mo
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Seeking Oncologist - Mercy Health Springfield, OH (near Dayton & Columbus)
Springfield, Ohio, United States
OnsiteFull Time
Seeking a medical oncologist to provide inpatient and outpatient oncology care, participate in clinical trials, and manage an average caseload of ~18-20 patients/day in an integrated cancer center.
3w
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Clinical Research Coordinator
Kettering, Ohio, United States
OnsiteFull Time
Coordinate clinical trials from start-up to closeout, maintain regulatory compliance (GCP/IRB/FDA), manage regulatory documents, enroll participants, process specimens, and use EMR/EDC and Microsoft Office.
EMR, EDC, Vendor Portals, Microsoft Word, Microsoft Excel, Microsoft Outlook, OneDrive, Teams
1mo
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Clinical Research Coordinator II
Cincinnati, Ohio, United States
OnsiteFull Time
3+ YOE3+ years clinical research coordination experience, knowledge of GCP and FDA regulations, able to manage multiple trials, perform blood draws/ECGs/specimen processing, obtain informed consent, and maintain regulatory documentation.