About Us:
Indomo is a clinical stage therapeutics company transforming clinic-based procedures into at-home care via device-enabled therapeutics. Indomo’s lead program couples a proven corticosteroid with an innovative intradermal self-injection device to create the first fast-acting at-home solution for inflammatory acne lesions.
Position Overview:
We are seeking a highly analytical MD or PhD-level researcher (e.g., medicine, pharmacology, biomedical sciences) to conduct a structured landscape analysis of drugs delivered via intradermal or intralesional injection, including both on-label and off-label use cases.
This role is ideal for a graduate student, resident, fellow, or early-career scientist with strong literature review and synthesis skills who is comfortable translating clinical and medical data into actionable insights.
Key Responsibilities:
Landscape Mapping
Identify and catalog drugs delivered via intradermal and/or intralesional injection (approved, off-label, and in trials)
Synthesize findings into structured tables and summaries
Opportunity Assessment
Evaluate and prioritize high-potential opportunities based on:
Market size / patient population
Reimbursement vs. cash-pay dynamics
Frequency of treatment / repeat use
Assess strength of clinical evidence and safety profile
Deep-Dive Analyses on Specific Drugs & Indications
Review and summarize
Published clinical data (RCTs, case series, meta-analyses)
Ongoing or recent clinical trials
Extract key treatment parameters
Depth of injection
Volume of injection
Number of injections per session
Treatment frequency
Highlight gaps, inconsistencies, and opportunities for innovation
Deliverables:
Structured dataset (Excel/Google Sheets) of drugs and indications
Slide deck or memo summarizing:
Key insights
Top opportunities
Supporting evidence
Deep-dive briefs on prioritized indications/drugs
Source-backed references (PubMed, clinical trials, guidelines, etc.)
Qualifications:
MD, PhD, or equivalent (or currently enrolled in program)
Background in dermatology, immunology, pharmacology, or oncology preferred
Strong experience with:
Literature reviews (PubMed, clinicaltrials.gov)
Clinical data interpretation
Ability to distinguish high-quality vs. weak evidence
Excellent written communication and structured thinking
Self-directed and detail-oriented
Able to work with minimal guidance and iterate quickly
Comfortable synthesizing ambiguity into clear insights
Duration: Initial project (6–12 weeks) with potential for extension
Hours: Flexible (5–10 hrs/week expected)
Compensation: $50 - $100 / hour (range depending on experience)
We are focused on building a diverse and inclusive workforce. If you’re excited about this role, but do not meet 100% of the qualifications listed above, we encourage you to apply.
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