
201 - 500 employees
🏥 Healthcare
💼 Consulting
⚕️ Healthcare Insurance
Healthcare • Consulting • Healthcare Insurance
Sitero is a next-generation clinical trial solutions provider that accelerates clinical trials, ensures compliance and safety, and enables innovation through advanced technology and world-class services. They offer a wide range of clinical services, including site support and activation, data management, biostatistics, and drug safety. Sitero specializes in eClinical technology, providing end-to-end, technology-enabled services such as electronic data capture, randomization and trial supply management, clinical trial management systems, electronic consent solutions, and payment systems. Their services also include IRB ethical review, biosafety consulting, and pharmacovigilance agreements, ensuring comprehensive support for clinical research organizations.
🔥 11 minutes ago
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201 - 500 employees
🏥 Healthcare
💼 Consulting
⚕️ Healthcare Insurance
Healthcare • Consulting • Healthcare Insurance
Sitero is a next-generation clinical trial solutions provider that accelerates clinical trials, ensures compliance and safety, and enables innovation through advanced technology and world-class services. They offer a wide range of clinical services, including site support and activation, data management, biostatistics, and drug safety. Sitero specializes in eClinical technology, providing end-to-end, technology-enabled services such as electronic data capture, randomization and trial supply management, clinical trial management systems, electronic consent solutions, and payment systems. Their services also include IRB ethical review, biosafety consulting, and pharmacovigilance agreements, ensuring comprehensive support for clinical research organizations.
• Oversee one or more clinical trials • Ensure that project milestones are met on time, within budget, and in compliance with best practices • Develop and manage project plans, timelines, and budgets for clinical trials • Ensure compliance with regulatory guidelines and organizational goals • Lead and coordinate cross-functional teams • Design and execute study plans and protocols • Manage study budgets • Prepare and submit necessary documentation to regulatory authorities • Supervise trial sites and various teams involved in clinical trial operations • Coordinate trial tasks and timelines • Oversee patient recruitment • Collaborate with Project managers to establish targets • Train and mentor Clinical Trial Managers, Clinical Research Associates, and Clinical Trial Associates
• Bachelors Degree or 6 years relevant experience with a CRO, Biotech, or Pharma Manufacturer • At least 3 years in a clinical trial management role • Previous experience CRA experience independently monitoring drug trials is highly preferred • Experience with CNS (Central Nervous System) drug trials is highly preferred
• competitive salary • Variable pay • paid time off • healthcare benefits • retirement benefits
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