Sr. Director, Translational Medicine Lead, Autoimmune
BioSpace · Cambridge, MA · 1 mo ago
OTHR$197k–$353k/yrFull-time
We need to output HTML fragment with sections: headings for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We must not repeat job title as heading. We must include sections only when posting has real specific content. We need to extract content.
The posting includes:
- The Role (description) -> could be "About the role" or "Responsibilities". The text after "Here's What You’ll Do" is responsibilities. Also earlier paragraph about leading translational strategy etc is also role description. We can combine into a "Responsibilities" section.
- Here’s What You’ll Need (Basic Qualifications) -> Requirements/Qualifications.
- Here’s What You’ll Bring to the Table (Preferred Qualifications) -> could be "Preferred Qualifications" or "Skills". We'll treat as "Preferred Qualifications".
- Our Working Model -> maybe "Work Schedule" or "Schedule". It mentions 70/30 work model, in-office, etc. That's schedule info.
- Pay & Benefits -> includes benefits description and salary range. So we need Benefits and Pay sections. According to rules, we should only include Pay and Benefits sections if posting actually states them. It does: salary range and benefits list. So we need separate sections for Pay and Benefits? The instruction: "use
. Need to preserve all substantive information. Let's extract each responsibility sentence:
1. Lead clinical-facing translational strategy for multiple programs and/or the most scientifically complex and business-critical autoimmune assets, integrating disease biology, therapeutic mechanism, patient heterogeneity, pharmacology, biomarker evidence, safety, and clinical outcomes into coherent development strategies.
2. Define the evidence required to establish confidence in mechanism, biological activity, therapeutic window, differentiation, and probability of technical success; anticipate major translational uncertainties and establish focused evidence-generation strategies to resolve them.
3. Shape autoimmune portfolio and modality strategy by establishing common scientific frameworks for immune tolerance, immune reset, durability, relapse, and non-response, and by informing prioritization of programs and indications based on human biology, translatability, biomarker feasibility, and competitive differentiation.
4. Provide senior leadership in human translational immunology, establishing state-of-the-art approaches to evaluate pathogenic and regulatory T-cell biology, B-cell states, autoantibodies, innate immunity, antigen-specific responses, and immune networks in patients.
5. Advance cross-program biomarker and translational technology strategy, including standards for clinical immune monitoring and fit-for-purpose use of high-dimensional flow cytometry, antigen-specific functional assays, immune repertoire analysis, transcriptomics, proteomics, serology, HLA/genetic analysis, and tissue-based approaches.
6. Partner with Clinical and Quantitative Pharmacology to establish integrated PK/PD and exposure-response frameworks connecting dose to target engagement, immune-cell effects, disease biology, safety, and clinical outcomes, including induction, maintenance, retreatment, or boosting strategies where relevant.
7. Shape translational safety strategy by anticipating risks from novel immune biology and integrating mechanistic monitoring into development plans; provide senior scientific leadership in interpreting relationships between efficacy-driving pharmacology and safety.
8. Serve as a senior translational voice in program and portfolio governance, presenting and defending recommendations concerning mechanism, patient population, dose, proof-of-concept, indication expansion, Go/No-Go criteria, and translational probability of success.
9. Lead cross-program reverse translation by identifying patterns across clinical programs, building feedback loops between human data and Research, and ensuring clinical observations influence target selection, modality design, next-generation programs, and portfolio-level understanding of mRNA/LNP behavior in autoimmune applications.
10. Build scientific capability and talent by mentoring Directors, Associate Directors, and scientists; establishing best practices; identifying capability gaps; and leading selected cross-functional initiatives that improve scientific quality, consistency, and speed across Translational Medicine.
11. Lead external scientific engagement with investigators and experts in autoimmune disease, immunology, and translational medicine; represent Moderna in scientific collaborations and appropriate external forums; drive high-impact publication strategies; and support evaluation of external technologies, partnerships, and innovation.
12. Additional duties as may be assigned from time to time.
We'll keep all.
Then . Let's extract:
- PhD, MD, MD/PhD, PharmD, or equivalent advanced degree in immunology, autoimmune disease, translational medicine, or a related discipline.
- Typically 10+ years of relevant scientific and drug-development experience following advanced training, with substantial biotechnology/pharmaceutical and/or human translational medicine experience.
- Demonstrated track record leading translational strategy for multiple clinical-stage immune-mediated or autoimmune programs.
- Broad and deep expertise in human immunology and autoimmune disease mechanisms, including strong command of adaptive and innate immunology, T-cell regulation, B-cell and autoantibody biology, antigen presentation, and inflammatory signaling.
- Extensive experience with clinical biomarker strategy and biomarker-rich clinical trials, with demonstrated ability to translate complex immune mechanisms and clinical and translational datasets into dose, patient population, proof-of-concept, lifecycle, and other development decisions.
- Strong understanding of the end-to-end drug-development process and how translational evidence influences clinical, regulatory, and portfolio strategy.
- Demonstrated ability to lead and influence senior stakeholders in complex matrix environments, mentor scientific talent, and communicate effectively at executive level.
We'll keep as list.
Then .
We should not include "About Moderna" section (the later paragraph about Moderna mission) because it's somewhat boilerplate but could be considered "About the role"? Already we have About the role. The later Moderna description is more about company; could be omitted as not required. The instruction says to remove boilerplate like EEO etc. This is not exactly boilerplate but could be considered company overview. However we already have About the role; we could include a short paragraph about Moderna mission under "About the role" or separate "About Moderna". But the allowed headings list does not include "About the company". So better to omit to avoid extra section. The content is not critical to the role; but it's substantive. However we could incorporate into "About the role" as extra paragraph. But we already have a paragraph about role; adding more may be okay. But to keep sections minimal, we could add another paragraph under About the role after the first paragraph. That would be okay.
Thus About the role will have two paragraphs: first as earlier, second about Moderna mission and values.
Let's extract that paragraph: "Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets