Sitero
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.
201 - 500 employees
⚕️ Healthcare Insurance
💊 Pharmaceuticals
☁️ SaaS
Senior Clinical Research Associate – Contract
Job not on LinkedIn
November 26
Sitero
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.
201 - 500 employees
⚕️ Healthcare Insurance
💊 Pharmaceuticals
☁️ SaaS
📋 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 to ensure timely site selection and feasibility • Ability to identify protocol deviations and pharmacovigilance issues that might affect data accuracy or patient safety • Conduct Site qualification, site initiation, routine site monitoring close out visits (remote and onsite) • Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation to identify trends, errors, and any potential breeches that can impact data integrity • Assists the Global Project Lead in identification of out-of-scope activities
🎯 Requirements
• 5 years of experience independently monitoring clinical drug trials • Completed at least 2 clinical trial application submissions in the past 5 years in each country pertinent to your contract • Rare Disease; Hepatology and Gastrology experience required • Bachelors degree in a life science field required
🏖️ Benefits
• competitive salary • Variable pay • paid time off • healthcare benefits • retirement benefits
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