ResearchEd
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.
education research • public policy • community college • rural education • Postsecondary Data Partnership
Senior Clinical Research Associate
March 15
ResearchEd
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.
education research • public policy • community college • rural education • Postsecondary Data Partnership
📋 Description
• Monitor clinical trial programs and manage regional clinical trial sites to support biological and pharmaceutical developmental programs. • Collaborate with assigned clinical research team on site selection and study initiation procedures. • Travel up to 80% within assigned territory for clinical trials. • Conduct or assist with site evaluations, study initiations, routine monitoring, site close-outs, and FDA audit preparations.
🎯 Requirements
• 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.
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