Research Administration Management Analyst-Medical Oncology

The Ohio State University • Columbus, OH

7d • Onsite

About The Position

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 IIT Research Administrative Management Analyst is involved in all facets of clinical trial conduct from initial protocol development including identification of potential sponsors/funders, through trial closure and project completion with limited supervision, increased independence and limited assistance; 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 functions to ensure the scientific integrity of the data collected, and the protection of the rights, safety, and well-being of human study subjects. The IIT Research Administrative Management Analyst clinical trial role includes administration, financial and billing management, consultation, education, data management (abstraction, reporting, analysis, monitoring, auditing), ethics and regulations, liabilities and responsibilities of conducting 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 and documentation in patient-centered research to accomplish these goals.

Requirements

• A Bachelor's degree in business administration, communications, marketing, or other relevant healthcare field or an equivalent combination of education and experience required.
• 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.

Nice To Haves

• Master's degree preferred.
• Experience in health professions research preferred.

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 functions to ensure the scientific integrity of the data collected, and the protection of the rights, safety, and well-being of human study subjects.
• Manages administration, financial and billing aspects of clinical trials.
• Provides consultation and education related to clinical trials.
• Manages data abstraction, reporting, analysis, monitoring, and auditing.
• Ensures compliance with ethics and regulations for 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 and documentation in patient-centered research.

Benefits

• Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
• Paid time off, including sick and vacation time and 11 holidays.
• State retirement plan or an alternative retirement plan, both with generous employer contributions.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level