Part-Time Medical Researcher

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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