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 the life cycle of clinical trial • Study start up support, site activation, trial conduct and closeout of a clinical trial • Provides support to the Global Project Lead and CTM during project start up • Assists with collection of essential documents from the site • Ability to identify protocol deviations and pharmacovigilance issues • Conduct Site qualification, site initiation, routine site monitoring close out visits • Expert documentation of monitoring priorities/activities • Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation • Ability to present essential function of CRA role in Bid Defenses, Investigator Meetings, and Sponsor Face to Face meetings • Provides support to the CTM and Global project lead in negotiation of site budgets and contracts
🎯 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 • Bachelor's degree in a life science field required
🏖️ Benefits
• competitive salary • Variable pay • paid time off • healthcare benefits • retirement benefits
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