The Francis S. Collins Scholars Program is for talented post-doctoral researchers or early-career faculty members looking to make a significant impact in clinical and translational research for NF1.
Named for the pioneering scientist who led a team that discovered the NF1 gene in 1990, The Francis S. Collins Scholars Program accepts applications from candidates who are committed to advancing the frontiers of NF1 research and clinical care. This highly competitive program, which was launched in 2014, has inducted close to 20 clinician scientists who now hold positions of leadership in the field. It provides formal training in clinical and translational science, mentorship from leaders in NF1 and related fields, and clinical training for the care of patients with NF1.
As a Francis S. Collins Scholar, you will receive up to 100% salary support for NF1-associated clinical, research, educational and mentorship activities.
This is a career-changing opportunity to join a community of scientists committed to making a lasting impact in NF1 research and clinical care.
Funding, mentoring and resources
NTAP is laser-focused on accelerating treatments for:
Plexiform neurofibromas (PN)
Cutaneous neurofibromas (cNF)
NF1 tumor biology and therapeutic vulnerabilities
Projects must show a direct path toward therapy development.
Commonly funded areas:
Drug discovery or drug repurposing
Biomarker discovery for therapeutic monitoring
Preclinical models testing treatment response
Molecular pathways that drive PN or cNF
Therapeutic target validation
Translational studies linking patient samples to therapy development
❗ Predictor: If a proposal is not directly linked to creating or advancing a therapy, it rarely succeeds.
NTAP regularly communicates strategic focus areas such as:
Model systems enabling therapy development (organoids, PDX, genetic models)
Response biomarkers for trials
Drug screening platforms
Cutaneous neurofibroma treatment pathways
Combination therapy rationales
Mechanisms of resistance to MEK inhibitors (e.g., selumetinib)
Clinical trial-enabling studies
Predictor: Align your proposal with a clearly identified NTAP strategic gap, not a generic NF1 study.
NTAP expects evidence that:
The model or system works
The therapeutic target is promising
Pilot efficacy data supports further testing
Human tissue or cell access is secured
Necessary collaborations are in place
Predictor: Robust pilot data is one of the strongest indicators of competitiveness.
NTAP is not a basic research foundation.
Successful applications show:
A defined translational endpoint (e.g., drug lead, biomarker, trial-ready intervention)
Work that can move quickly into IND-enabling or clinical feasibility steps
A timeline that fits within 1–2 years for concrete outcomes
Predictor: Translational relevance is essential.
Strong proposals leverage:
NF1 patient-derived cells
cNF or PN tissue samples
NF1 organoids, spheroids, or engineered systems
NF1 mouse models (e.g., Nf1 floxed lines, Dhh-Cre, Prss56 models)
Data from natural history studies or clinical cohorts
Predictor: Use of disease-relevant, validated NF1 models significantly boosts competitiveness.
NTAP-funded projects typically include:
2–3 tightly scoped aims
Milestone-based design (go/no-go gates)
Well-defined preclinical endpoints
Short timelines with feasible execution
Risk mitigation strategies
Predictor: Concrete deliverables and milestones are highly valued.
NTAP is deeply collaborative and encourages:
Multi-PI or multi-institution teams
Integration of molecular biology + pharmacology + clinical insights
Partnerships with NF clinical trial consortia
Shared data and resource plans
Predictor: Proposals with cross-disciplinary and multi-site teams score higher.
Funded projects often articulate:
A critical unmet need (e.g., few options for cNF treatment)
How the project accelerates therapy timelines
How outcomes will affect NF1 patient care
Pathways for future clinical translation
Predictor: Patient-centered framing improves impact score.
Successful applications demonstrate:
Access to NF1 clinical cohorts
Access to patient samples
Bioinformatics, pharmacology, or imaging cores
Departmental support, protected time, and infrastructure
Predictor: Strong environment increases reviewer confidence.
Top-scoring NTAP proposals:
Are very clear and concise
Provide strong visual preliminary data
Explain rationale in NF1 context, not general cancer biology
Make translational impact explicit
Clearly outline expected therapeutic acceleration steps
Predictor: Clear storytelling elevates scoring and enthusiasm.
| Predictor | Why It Matters |
|---|---|
| Direct NF1 therapeutic relevance | Core mission requirement |
| Alignment with NTAP priorities | Ensures reviewer excitement |
| Strong preliminary data | Demonstrates feasibility |
| Translational/preclinical focus | NTAP is therapy-driven |
| NF1-relevant models | Ensures human relevance |
| Clear, milestone-driven aims | Fits NTAP project structure |
| Collaborations | Enhances impact and feasibility |
| Patient-centered justification | Aligns with mission impact |
| Strong environment | Supports execution |
| Clear writing | Improves reviewer enthusiasm |
Sponsor Institute/Organizations: Neurofibromatosis Therapeutic Acceleration Program
Sponsor Type: Corporate/Non-Profit
Address: 600 North Wolfe Street, Meyer 8-149, Baltimore, MD 21287.
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Dec 08, 2025
Dec 08, 2025
$25,000
Affiliation: Neurofibromatosis Therapeutic Acceleration Program
Address: 600 North Wolfe Street, Meyer 8-149, Baltimore, MD 21287.
Website URL: https://www.n-tap.org/for-researchers/francis-s-collins-scholars-program
Disclaimer:It is mandatory that all applicants carry workplace liability insurance, e.g., https://www.protrip-world-liability.com (Erasmus students use this package and typically costs around 5 € per month - please check) in addition to health insurance when you join any of the onsite Trialect partnered fellowships.