Clinical Science Consultant

 Posted a day ago
     
 $200 - $400 per hour
  
10+ years experience
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AI Summary

Serve as a subject matter expert to define the gold standard for AI-generated clinical content and ensure outputs are scientifically sound and regulatory-compliant. Activities include sharing domain knowledge on regulatory submissions, reviewing ground-truth artifacts, and identifying AI value-add opportunities in clinical workflows.

About
Edison Scientific builds and commercializes AI agents for science. Scientific discovery moves too slowly, and autonomous AI agents are how we intend to fix that. We're assembling a team of top researchers and engineers across AI and biology to build an AI scientist.

The Opportunity
We are seeking an experienced Clinical Science Consultant for a flexible, part-time engagement. You'll serve as the subject matter expert who defines the gold standard for AI-generated clinical content and outputs — ensuring our platform produces work that is scientifically sound, clinically meaningful, and aligned with current regulatory expectations.

We engage directly with domain experts to help design and build these capabilities, and to surface what we don't yet know. Your insights will help ensure we're solving the right problems for clinicians and development teams in the field.

Day to day that might look like any or all of the following sorts of activities (and more):

  • Knowledge sharing about "day-in-the-life" as an expert working with data in these domains to assemble regulatory submissions.

  • Describing common tasks or problems where AI could be of value in your workflows.

  • Identify + describe internal pharma systems that are commonly used for standard workflows.

  • Generate or review reference ground-truth artifacts to evaluate against - reports, data files, modules, etc.

  • Identify + add realistic sources of variance or data corruption in study data.

  • Identify and correct discrepancies in data quality.

Qualifications

  • 10+ years of experience in clinical science or clinical development within the pharmaceutical/biotechnology industry, ideally with a sponsor.

  • Bachelor's degree in a life sciences discipline required; advanced degree (MD, PhD, or PharmD) preferred.

  • Hands-on experience designing and executing early-phase (Phase I and/or Phase II) clinical trials, including protocol development, endpoint selection, and study operational planning.

  • Strong working knowledge of FDA and ICH guidelines governing clinical trial design and conduct, with experience contributing to or reviewing IND submissions.

Why join us?

  • Remote/US based

  • Flexible hours / flexible time zone - 5-20 hours per week

Note: For consulting opportunities, we do not offer benefits.

Why join us?

  • Competitive salary and equity

  • Full healthcare coverage — we pay 100% of premiums for you and your dependents

  • Support for growing families, including a yearly new parent stipend and fertility coverage through Carrot

  • Mental health support through Rula, our in-network therapist and psychiatrist network with fast availability

  • 12 weeks of paid parental leave for maternity, paternity, and adoption

  • Pet care support with a yearly employer-funded stipend for your animal companions

  • Commuter benefits so you can pay for transit and parking with pre-tax dollars

  • 401(k) company matching

  • $300 health and wellness benefit quarterly

  • Lunch is on us every day you're in the office, and dinner is on us when you're working late

  • Regular team offsites and company events

  • A fast-moving, mission-driven culture where smart people do their best work and actually enjoy doing it

Edison Scientific is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected characteristic under applicable law.

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