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RAPTIC

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RAPTIC

RAPTIC supports faculty doing innovative research in the medical, health or biomedical fields. 

RAPTIC Program Mission

Facilitate and accelerate progress in translational and clinical research at Ohio State by increasing awareness of and access to key resources and training, in order to identify and realize innovative ideas with applications that can be protected by IP, funded, commercialized and implemented in healthcare or biomedical settings.

RAPTIC is a year-long program; participant applications open in July each year, learning sessions run September to May, and every other June we hold a showcase and pitch competition. 

1 Short-Term Goals

  • Faculty recruitment, retention, job satisfaction
  • Support more ‘projects’ turning into ‘products’ at Ohio State
  • Connect faculty and their research teams to resources and information that enable the innovation pipeline 
  • Encourage cross-campus collaborations and peer support
  • Accelerate research progress and success for a broad group of faculty

2 Longer-Term Goal

  • Improve metrics for faculty research, IP, licensing, innovation grants and retention collectively driving a higher return on investment for individual colleges through existing fiscal workflows on campus that return indirects, license revenue, industry co-development opportunities and more.

“My confidence grew so much and I learned the research building blocks I needed.”

RAPTIC Pilot Cohort Participant

Three Phases of RAPTIC

Faculty may join at the appropriate phase. 

1 Ideation to Innovation

Strengthening research programs, transforming research ideas into innovative concepts, learning about IP.

2 Projects to Products

Developing projects into tangible products while securing intellectual property.

3 Invention Development

Refining inventions, mitigating risks, and planning for business success.

Key Elements of Each Phase

“I never would have submitted this grant if I didn’t have the support of RAPTIC.”

RAPTIC Pilot Cohort Participant

R34/U01 Clinical Trials Deliverables Project Management

Appendix B: R34/U01 Clinical Trials Deliverables- Project Management

There is an illustration of a building shape with pillars. At the top of the building share is a triangle shaped roof with UM1 Submission in text. The next layer has the words "Regulatory Authority Submission Management."

There are nine pillars holding the roof in place and the read from left to right: Data Management Plan (CRF); Statistical Plan; HSP- Informed Consent (transitions); Drug Supply/Accountability; Monitoring Plan; Enrollment, Randomization & Subject Tracking; Central Laboratory & Sample Repository; Data Safety and Monitoring Plan; Training and Site Initiation Plan.

Below these nine pillars are four levels of flooring, which include form the top to the bottom: Sites/Subcontracts/budgets, Clinical Operations Management and Manual of Procedures, Study team, and lastly, Protocol and Investigator Brochure. 

Clinical Research Team Structure (Page 13)

Appendix A: Clinical Research Team Structure (Page 13)

The Clinical Research Team Structure image illustrates the hierarchical organization and roles within a clinical research team. The structure is designed to ensure efficient management and execution of clinical trials. Here is a detailed description of the image:

Regulatory (ICH, FDA) is in a black box positioned at the top center of the hierarchy with the Sponsor and Contract Research Organization branching out directly below in gray boxes. Underneath is the Medical Director in a spruce green box with a Coordination Center beige box branching out below and to the left that includes purple boxes with Regulatory sStaff, Fiscal management and a Project Manager. Branching out below and to the right is the Data Coordinating Center in the same style beigh box as the Coordination Center that includes Data Manager, Statistician and Monitor in mustard yellow boxes.

The next tier on the structure has the Principal Investigator in a lime green box positioned at the top middle of this next level of hierarchy with the Grants Manager, Sponsored Programs, IRB and CCRM/CTO Management Teams listed next to it in pink boxes. 

Below this tier are gray arrows that show a back and forth connection with the Principal investigator lime green box is a row of teal boxes that include, from left to right, Research Assistant, Nurses, lab Tech, Clinical Research Coordinator, Sub-investigators and Pharmacist. 

Directly below these teal boxes is one sky blue box with an arrow showing the back and forth relationship with Subjects.

 

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