
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.
🔥 9 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 and 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 • Lead and coordinate cross-functional teams, including clinical research associates, data managers, and other stakeholders • Ensure that all clinical trials adhere to Good Clinical Practice (GCP) and other regulatory requirements • Train and mentor Clinical Trial Managers, Clinical Research Associates, and Clinical Trial Associates
• Bachelor's Degree or 6 years relevant experience with a CRO, Biotech, or Pharma Manufacturer • At least 3 years in a clinical trial management role • Previous 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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