Intern, Non-Clinical Safety

Praxis

. Review, organize, and assign metadata to reports from in vitro Drug Metabolism and Pharmacokinetics (DMPK) studies .

Posted 11/4/2026part-timeRemote • United StatesEntry Level💰 $22 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates strong organizational skills and attention to detail in managing and documenting scientific information, with proficiency in Microsoft Office and experience in non-clinical development processes, particularly in Drug Metabolism and Pharmacokinetics.

Highest-signal resume keywords

Project ManagementData OrganizationMicrosoft Office ProficiencyCollaboration SkillsLaboratory Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Metadata ManagementDashboard DevelopmentDatabase ManagementSpreadsheet ProficiencyScientific Documentation

Soft Skills

Strong Written CommunicationAttention to DetailCuriosityMotivation to LearnAbility to Prioritize

Tools & Technologies

SmartsheetMicrosoft Office

Industry Keywords

In Vitro Drug MetabolismPharmacokineticsNon-Clinical DevelopmentToxicologyPharmaceutical Industry

About the role

Key responsibilities & impact

Review, organize, and assign metadata to reports from in vitro Drug Metabolism and Pharmacokinetics (DMPK) studies
Build and maintain a dashboard or tracking tool providing visibility into the status of in vitro DMPK studies
Take ownership of assigned projects, manage work against agreed timelines, and provide regular updates on progress and roadblocks
Support continuous improvement projects across Non-Clinical Development, including Toxicology, Drug Metabolism, and Pharmacokinetics
Work with colleagues across the Non-Clinical team to understand how scientific data and studies contribute to the broader drug development process
Identify opportunities to improve the organization, accessibility, and usefulness of Non-Clinical information and tools

Requirements

What you’ll need

Currently enrolled as a junior or senior in a bachelor’s degree program in life sciences or a related field
Strong written communication skills and attention to detail, particularly when organizing and documenting scientific information
Comfortable working with databases and/or spreadsheets
Proficiency with Microsoft Office is required
Experience with Smartsheet is preferred
Able to organize and prioritize work, stay focused, and independently move assigned projects forward while knowing when to ask for help
Curious and motivated to learn about non-clinical development and the pharmaceutical industry
Able to collaborate effectively with colleagues across different scientific and functional areas
Laboratory experience is preferred, particularly exposure to in vitro Drug Metabolism and Pharmacokinetics work

Benefits

Comp & perks

99% of the premium paid for medical, dental and vision plans
Company-paid life insurance
AD&D benefits
Disability benefits
Voluntary plans to personalize coverage
Dollar-for-dollar 401(k) match up to 6% on eligible contributions
Long-term stock incentives
ESPP
Discretionary quarterly bonus
Extremely flexible wellness benefit
Generous PTO
Paid holidays
Company-wide shutdowns