Investigator-Initiated Studies and Services
At the TGH Office of Clinical Research (OCR), our team is dedicated to supporting researchers throughout the entire research process. We offer support and guidance on a wide range of services, including:
- Protocol Development: Assistance with formulating a clear and focused research question and refining your research protocol. We also provide support and guidance in selecting appropriate study design and methods and data collection tool.
- Regulatory and IRB Submission Process and Approvals: Step-by-step guidance on navigating the regulatory and IRB submission requirements based on each study type.
- Data Analysis and Interpretation: This service is provided on request for biostatistical services and/or for funded studies. We can provide basic guidance on who to contact and what will be needed for the analysis of your study.
- Abstract and Manuscript Writing: Advice on structuring and writing your manuscript for publication.
Please note: We provide ONLY guidance and support for Investigator-Initiated studies but do not offer medical or grant writing services at this time.
For any assistance or inquiries regarding retrospective studies, please reach out to our team:
Sadaf Aslam, MD, MS, saslam@tgh.org, saslam@usf.edu
Veronique Perry, MBA, DHA, vperry@tgh.org