First Name:
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Last Name / Surname:
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Date of Birth:
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M-D-Y
Preferred email:
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Citizenship:
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U.S. Citizen
U.S. Permanent Resident
Foreign Citizen
Do you currently have a Ph.D., M.D., or other doctoral degree in a related discipline?
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Yes
No
The TSIF fellowship is only open to those who have completed their terminal doctoral degree up to two years before the start year of the fellowship. Did you receive your terminal degree (a Ph.D., M.D., or other doctoral degree in a related discipline) in 2023 or after?
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Yes
No
Will you have a Ph.D., M.D., or other doctoral degree in a related discipline before the start of the fellowship (Sept. 8th, 2025)?
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Yes
No
I confirm that I have read and understand the FDA Ethics for Nonemployee Scientists requirements.
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Please select your first choice project:
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Developing State-of-the-Art Analytical Methods for the Comparison of Biosimilar Drugs to Related Human Growth Hormones Mentors: Kan Chen (CDER/FDA), Christopher LeClair (NCATS) and Dingyin Tao (NCATS)
Leveraging AI to Enhance Drug Safety Predictions through Integrated Analysis of Tox21 Data and FDA's Clinical Data Mentors: Minjun Chen (NCTR/FDA) and Ruili Huang (NCATS)
Enhancing Intestinal Barrier Research through Integrative High-Throughput TEER Analysis and Mechanistic Elucidation for Intestinal Toxicity Screening Mentors: Sangeeta Khare (NCTR/FDA), Kuppan Gokulan (NCTR/FDA), Xin Xu (NCATS) and Elias Carvalho Padilha (NCATS)
Quantitative high throughput screening for drugs targeting COP1 to promote T cell function. Mentors: Weiming Ouyang (CDER/FDA) and Menghang Xia (NCATS)
Understanding the implications of codon optimization on the physiochemical and immunogenic properties of truncated-ADAMTS13 (MDTCS) and Niemann-Pick disease Mentors: Chava Kimchi-Sarfaty (CDER/FDA) , Upendra Katneni (CBER/FDA) and Catherine Chen (NCATS)
Evaluation of three-dimensional (3D) immunocompetent skin fibrosis model for cell-based therapy products Mentors: Kyung Sung (CBER/FDA), Mark Ferrer (NCATS) and Yi Wei Lim (NCATS)
Development of a defined process for manufacturing iPSC-derived mesenchymal stromal cells producing extracellular vesicles to modulate pericyte function in neurodegenerative disease Mentors: Ross Marklein (CBER/FDA), Jin Han (CBER/FDA), Carlos Tristan (NCATS)
Developing 3D Bioprinted Outer Blood Retina Barrier Model of Choroideremia Using Patient-derived iPSCs for Assessing Gene Therapy Safety and Efficacy Mentors: Ronit Mazor (CBER/FDA) ,Zhaohui Ye (CBER/FDA), Sojin Bing and Min Jae Song (NCATS) Collaborators: Ruchi Sharma (NEI) and Kapil Bharti (NEI)
Please select your second choice project:
* must provide value
Developing State-of-the-Art Analytical Methods for the Comparison of Biosimilar Drugs to Related Human Growth Hormones Mentors: Kan Chen (CDER/FDA), Christopher LeClair (NCATS) and Dingyin Tao (NCATS)
Leveraging AI to Enhance Drug Safety Predictions through Integrated Analysis of Tox21 Data and FDA's Clinical Data Mentors: Minjun Chen (NCTR/FDA) and Ruili Huang (NCATS)
Enhancing Intestinal Barrier Research through Integrative High-Throughput TEER Analysis and Mechanistic Elucidation for Intestinal Toxicity Screening Mentors: Sangeeta Khare (NCTR/FDA), Kuppan Gokulan (NCTR/FDA), Xin Xu (NCATS) and Elias Carvalho Padilha (NCATS)
Quantitative high throughput screening for drugs targeting COP1 to promote T cell function. Mentors: Weiming Ouyang (CDER/FDA) and Menghang Xia (NCATS)
Understanding the implications of codon optimization on the physiochemical and immunogenic properties of truncated-ADAMTS13 (MDTCS) and Niemann-Pick disease Mentors: Chava Kimchi-Sarfaty (CDER/FDA) , Upendra Katneni (CBER/FDA) and Catherine Chen (NCATS)
Evaluation of three-dimensional (3D) immunocompetent skin fibrosis model for cell-based therapy products Mentors: Kyung Sung (CBER/FDA), Mark Ferrer (NCATS) and Yi Wei Lim (NCATS)
Development of a defined process for manufacturing iPSC-derived mesenchymal stromal cells producing extracellular vesicles to modulate pericyte function in neurodegenerative disease Mentors: Ross Marklein (CBER/FDA), Jin Han (CBER/FDA), Carlos Tristan (NCATS)
Developing 3D Bioprinted Outer Blood Retina Barrier Model of Choroideremia Using Patient-derived iPSCs for Assessing Gene Therapy Safety and Efficacy Mentors: Ronit Mazor (CBER/FDA) ,Zhaohui Ye (CBER/FDA), Sojin Bing and Min Jae Song (NCATS) Collaborators: Ruchi Sharma (NEI) and Kapil Bharti (NEI)
No second choice project. Only consider me for my first choice project.
Please select your third choice project:
* must provide value
Developing State-of-the-Art Analytical Methods for the Comparison of Biosimilar Drugs to Related Human Growth Hormones Mentors: Kan Chen (CDER/FDA), Christopher LeClair (NCATS) and Dingyin Tao (NCATS)
Leveraging AI to Enhance Drug Safety Predictions through Integrated Analysis of Tox21 Data and FDA's Clinical Data Mentors: Minjun Chen (NCTR/FDA) and Ruili Huang (NCATS)
Enhancing Intestinal Barrier Research through Integrative High-Throughput TEER Analysis and Mechanistic Elucidation for Intestinal Toxicity Screening Mentors: Sangeeta Khare (NCTR/FDA), Kuppan Gokulan (NCTR/FDA), Xin Xu (NCATS) and Elias Carvalho Padilha (NCATS)
Quantitative high throughput screening for drugs targeting COP1 to promote T cell function. Mentors: Weiming Ouyang (CDER/FDA) and Menghang Xia (NCATS)
Understanding the implications of codon optimization on the physiochemical and immunogenic properties of truncated-ADAMTS13 (MDTCS) and Niemann-Pick disease Mentors: Chava Kimchi-Sarfaty (CDER/FDA) , Upendra Katneni (CBER/FDA) and Catherine Chen (NCATS)
Evaluation of three-dimensional (3D) immunocompetent skin fibrosis model for cell-based therapy products Mentors: Kyung Sung (CBER/FDA), Mark Ferrer (NCATS) and Yi Wei Lim (NCATS)
Development of a defined process for manufacturing iPSC-derived mesenchymal stromal cells producing extracellular vesicles to modulate pericyte function in neurodegenerative disease Mentors: Ross Marklein (CBER/FDA), Jin Han (CBER/FDA), Carlos Tristan (NCATS)
Developing 3D Bioprinted Outer Blood Retina Barrier Model of Choroideremia Using Patient-derived iPSCs for Assessing Gene Therapy Safety and Efficacy Mentors: Ronit Mazor (CBER/FDA) ,Zhaohui Ye (CBER/FDA), Sojin Bing and Min Jae Song (NCATS) Collaborators: Ruchi Sharma (NEI) and Kapil Bharti (NEI)
No third choice project. Only consider me for my first, or first and second, choice projects.
If you are not accepted into the TSIF program, would you be interested in having your CV and application information forwarded for other NCATS postdoctoral opportunities?
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Yes
No
Name (First and Last) Email Phone Number 1 2 3
Curriculum Vitae (CV)
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Personal Statement: In narrative form, describe your research interests and goals and how these relate to the fields of translational science and regulatory and drug development science. Additionally, indicate how your goals are aligned with one or more of the TSIF projects listed on the TSIF web-page. Please also provide insight into your short- and long-term career goals, and explain how the TSIF program will help you in achieving those goals. Please limit your personal statement to two typed, single-spaced pages and use 12-point font and 1" margins (approximately 1,000 words).
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Proof of terminal degree: If you have already obtained your terminal degree by the date of this application, please upload a copy of your graduate transcript or diploma, here, as proof of the degree (Ph.D., M.D., etc.).
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Proof of graduation: If you have not obtained your terminal degree by the date of this application, please submit documentation here that you will obtain the degree before September 8, 2025, the start-date of the TSIF fellowship. Examples include but are not limited to: written assurance from dissertation committee chair (for Ph.D. candidates) or the dean of the school (for M.D. candidates).
* must provide value
Proof of citizenship: Permanent residents of the United States must submit proof of eligibility for citizenship. The I-551 stamp in a passport is acceptable; "Employment Authorization" documents are not acceptable.
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I certify that, to the best of my knowledge, the provided information is true and accurate.
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OMB# 0925-0761 Expiration Date: 07/31/2025 Collection of this information is authorized by The Public Health Service Act, Section 479 (42 USC 287). The information collected in this application will be used to facilitate the acceptance and onboarding of applicants. Rights of participants are protected by The Privacy Act of 1974. The information you provide will be included in a Privacy Act system of records, and will be used and may be disclosed for the purposes and routine uses described and published in the following System of Records Notice (SORN): 09-25-0014 - Clinical Research: Student Records, HHS/NIH/OD/OIR/OE. Participation is voluntary, and there are no penalties for not participating or withdrawing at any time. The information collected will be kept private to the extent provided by law. Names and other identifiers will not appear in any report. Information provided will be combined for all participants and reported as summaries. Public reporting burden for this collection of information is estimated to average 60 minutes per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of information. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to: NIH, Project Clearance Branch, 6705 Rockledge Drive, MSC 7974, Bethesda, MD 20892-7974, ATTN: PRA (0925-0761). Do not return the completed form to this address.
Selection for the fellowship will be based solely on merit, with no discrimination for non-merit reasons, such as race, color, gender, national origin, age, religion, sexual orientation, or physical or mental disability. NIH and FDA provide reasonable accommodations to applicants with disabilities. If you need reasonable accommodation during any part of the application and hiring process, please notify us. The decision on granting reasonable accommodation will be handled on a case-by-case basis.
THE NIH/NCATS AND FDA ARE EQUAL OPPORTUNITY EMPLOYERS.
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