Clinical Science Consultant
About The Position
Edison Scientific is seeking an experienced Clinical Science Consultant for a flexible, part-time engagement. The consultant will serve as the subject matter expert responsible for defining the gold standard for AI-generated clinical content and outputs. This role ensures the platform produces scientifically sound, clinically meaningful content that aligns with current regulatory expectations. The consultant will engage directly with domain experts to help design and build AI capabilities, identify knowledge gaps, and ensure the company is solving the right problems for clinicians and development teams. Activities may include knowledge sharing about expert workflows with regulatory submissions, describing tasks where AI can add value, identifying common internal pharma systems, generating or reviewing reference ground-truth artifacts for evaluation, identifying sources of variance or data corruption in study data, and correcting data quality discrepancies.
Requirements
- 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.
- 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.
- Experience contributing to or reviewing IND submissions.
Nice To Haves
- Advanced degree (MD, PhD, or PharmD) preferred.
Responsibilities
- Define the gold standard for AI-generated clinical content and outputs.
- Ensure the platform produces scientifically sound, clinically meaningful content aligned with current regulatory expectations.
- Engage directly with domain experts to help design and build AI capabilities.
- Surface knowledge gaps.
- Ensure the company is solving the right problems for clinicians and development teams.
- Share knowledge about "day-in-the-life" as an expert working with data in regulatory submissions.
- Describe common tasks or problems where AI could be of value in workflows.
- Identify and describe internal pharma systems commonly used for standard workflows.
- Generate or review reference ground-truth artifacts to evaluate against (reports, data files, modules, etc.).
- Identify and add realistic sources of variance or data corruption in study data.
- Identify and correct discrepancies in data quality.
Benefits
- 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
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What This Job Offers
Job Type
Part-time
Career Level
Senior
