Manage and coordinate oncology clinical research trials, including patient recruitment, protocol development, and data management. Oversee oncology trials and research projects. Develop research protocols and grant proposals. Perform patient evaluations and administer medications. Train and supervise staff. Ensure compliance with regulations through audits. Manage financial accounts and authorize purchases. Develop strategies for participant recruitment and retention. Interface with study sponsors and resolve queries. Monitor IRB submissions and respond to requests.
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Industry
Administrative and Support Services
Education Level
Associate degree
Number of Employees
1,001-5,000 employees