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Clinical Science Consultant

Edison Scientific
Remote

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Job Details

Contract
$200 - $400 an hour

Benefits

Commuter assistance
Paid parental leave
Health insurance
Flextime
Adoption assistance
Parental leave
401(k) matching
Flexible schedule

Qualifications

Biotechnology
Research project design
ICH guidelines
Bachelor's degree
Pharmaceutical company experience
Clinical quality assurance standards
Clinical trial support in drug product development
Pharmaceutical research experience
Operations planning

Full Job Description

Location

Remote available (U.S. Only)

Employment Type

Contract

Location Type

Remote

Department

ResearchScience Research

Compensation

$200 – $400 per hour

About us

Edison Scientific builds and deploys AI scientist agents to accelerate science and the development of new medicines. We are an ambitious team run by scientists and engineers from leading institutions across biology, physics, chemistry, and AI.

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 ensures 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?

We're a fast-moving, mission-driven culture where smart people do their best work and actually enjoy doing it. We also offer full-time employees the following:

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 off-sites and company events

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.

Apply Now

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