Sitero
201 - 500 employees
⚕️ Healthcare Insurance
💊 Pharmaceuticals
☁️ SaaS
Healthcare Insurance • Pharmaceuticals • SaaS
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.
Medical Director – Contract
🔥 0 minutes ago
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Sitero
201 - 500 employees
⚕️ Healthcare Insurance
💊 Pharmaceuticals
☁️ SaaS
Healthcare Insurance • Pharmaceuticals • SaaS
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.
📋 Description
• Provide strategic input into current and potential clinical projects • Support site investigators and manage the medical monitoring • Responsible for strategic input on potential projects that support proposal writing and bid-defense meetings • Support of data review and medical writing for protocols and study specific reports • Review and address site and CRA queries for inclusion/exclusion criteria • Prepare listings of protocol deviations and adverse events for regular meetings
🎯 Requirements
• Licensed MD or PhD • 2 years of experience working in clinical trials as a medical monitoring associate or equivalent relevant experience • Endocrinology Pediatrics (preferred) • Metabolic trial experience (preferred)
🏖️ Benefits
• Competitive salary • Variable pay • Paid time off • Healthcare benefits • Retirement benefits
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