
Education • Non-profit • Social Impact
ResearchEd is an education policy research nonprofit providing objective analysis, deep insights, and detailed recommendations for education institutions and research organizations seeking to support equitable student outcomes and promote community and economic development through education. ResearchEd conducts student-centered work, particularly focusing on underserved groups, and provides research, data capacity building support, and advocacy. Their mission is to empower action in education, aiming for equitable access to education as a catalyst for community success and social justice.
3 hours ago

Education • Non-profit • Social Impact
ResearchEd is an education policy research nonprofit providing objective analysis, deep insights, and detailed recommendations for education institutions and research organizations seeking to support equitable student outcomes and promote community and economic development through education. ResearchEd conducts student-centered work, particularly focusing on underserved groups, and provides research, data capacity building support, and advocacy. Their mission is to empower action in education, aiming for equitable access to education as a catalyst for community success and social justice.
• Monitor clinical trial programs and manage regional clinical trial sites. • Collaborate with an assigned clinical research team to provide input on site selection, study initiation procedures, conflict resolution, and audit responses. • Conduct or assist with site evaluations, study initiations, routine monitoring, site close-outs, and FDA audit preparations. • Effectively communicate all relevant findings with appropriate in-house personnel. • Develop territory to broaden selection of research study sites. • Manage work activities in a time and cost-effective manner to ensure budgetary guidelines and project timelines are met. • Participate in internal and/or external meetings to maintain current knowledge on regulations and guidelines.
• Bachelor’s degree in a science or health-related discipline or equivalent of 7 years industry experience. • Minimum of 5 years’ experience in clinical research with direct site monitoring experience with a sponsor company or CRO and 3 years of recent oncology clinical trial experience. • Strong knowledge of clinical trial monitoring, regulatory compliance, clinical research methodology and all applicable regulations and guidelines. • Strong organizational and time management skills and the ability to work independently. • Excellent communication and interpersonal skills. • Flexibility and ability to travel routinely to meet project requirements. • Strong knowledge of standard computer applications. • Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa.
• Maintains a home office if working remotely. • Travels up to 80% within an assigned territory.
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Senior Clinical Research Associate responsible for monitoring clinical trial sites and ensuring compliance. Focus on risk-based monitoring and data accuracy in clinical research processes.
🇺🇸 United States – Remote
💵 $82.8k - $135k / year
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🦅 H1B Visa Sponsor
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