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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