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.
Senior Clinical Research Associate
🔥 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
• Primary point of contact for site personnel during life cycle of clinical trial • Provides support to the Global Project Lead and CTM during project start up • Assists with collection of essential documents from the site • Conduct Site qualification, site initiation, routine site monitoring close out visits • Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation to identify trends
🎯 Requirements
• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field required • advanced degree (MS, MPH, PharmD, or PhD) preferred • Minimum of 5-10 years of clinical research experience • Demonstrated site management experience • Strong knowledge of GCP, regulatory requirements, and clinical trial operations • Oncology experience preferred
🏖️ Benefits
• competitive salary • paid time off • healthcare and retirement benefits
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