Research Administration Management Analyst-Medical Oncology

About the role

The IIT (Investigator Initiated Trial) Research Administrative Management Analyst acts on behalf of and under the direction of the sponsor-investigator(s) in the Division of Medical Oncology within the Department of Internal Medicine. The role involves all facets of clinical trial conduct from initial protocol development to trial closure and project completion with limited supervision.

Responsibilities

• Drafts and initiates investigator initiated clinical trials, including multicenter studies where OSU is the coordinating site.
• Trains study coordinators to effectively coordinate an investigator initiated study by providing guidance and internal monitoring.
• Oversees investigator-initiated clinical trials and ensures the scientific integrity of the data collected, and the protection of the rights, safety, and well-being of human study subjects.
• Administers, manages finances and billing for clinical trials.
• Consults on ethical and regulatory issues related to research involving human subjects.
• Designs, creates, implements, modifies, and maintains tracking systems, electronic and paper databases, data management facilities, and standard operational procedures for study patient participation and regulatory compliance.

Requirements

• A Bachelor's degree in business administration, communications, marketing, or other relevant healthcare field or an equivalent combination of education and experience required; Master's degree preferred.
• 2 years of relevant experience in patient-centered research (ideally including clinical trials), business, drug development, or other management capacity required.
• Experience with program management and development required.
• Experience in health professions research preferred.

Qualifications

• Strong organizational skills and attention to detail.
• Excellent communication and interpersonal skills.
• Ability to work independently and manage multiple projects simultaneously.
• Knowledge of clinical research protocols and regulations.
• Proficiency in Microsoft Office Suite and data management software.