FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in gene therapy, drug design, and AI agent evaluation within the genetic medicines pipeline, with a strong emphasis on scientific writing and regulatory knowledge.
Highest-signal resume keywords
Gene Therapy ExperienceDrug Design ExpertiseAI Agent ProficiencyRegulatory KnowledgeScientific Writing Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Gene EditingRNA TherapeuticsDrug ScreeningDose SelectionRisk AssessmentImmunogenicity EvaluationGLP Toxicology InterpretationPotency EvaluationSpecificity AssessmentDevelopability Trade-offs
Soft Skills
Proactive Problem-SolvingHigh AgencyInitiativeComfort Operating in Uncertainty
Certifications & Qualifications
Advanced Degree (MS/PhD/PharmD)
Industry Keywords
Genetic MedicinesIND-Enabling StudiesFDA/EMA Regulatory RequirementsNonclinical Data PackageTarget ValidationChemistry OptimizationCandidate Nomination
About the role
Key responsibilities & impact- Contribute to the technical approach for evaluating AI agent performance across the genetic medicines pipeline
- Design realistic program case studies spanning target validation, drug design and screening, chemistry optimization, candidate nomination, and IND-enabling studies
- Evaluate PK/PD, immunogenicity, and GLP toxicology findings across modalities and development stages
- Reconstruct program go/no-go decisions from multi-source data
- Review and stress-test agent outputs for scientific soundness
- Identify reasoning that is textbook-correct but not defensible in a program review
- Calibrate AI agent confidence on preclinical data with incomplete or conflicting signals
- Work with software engineers and scientists to build datasets and AI agent tasks across the end-to-end genetic medicines pipeline
Requirements
What you’ll need- Advanced degree (MS/PhD/PharmD) in molecular biology, genetics, gene therapy, or a related biomedical field, or equivalent industry experience
- 3+ years of hands-on experience in gene therapy, gene editing, or RNA therapeutics (ASO/siRNA/mRNA) discovery or development
- Direct experience with drug design, drug screening, delivery optimization, or IND-enabling study design in at least one genetic medicine modality
- Experience interpreting on-/off-target editing data, biodistribution, immunogenicity, and GLP toxicology to inform dose selection and risk assessment
- Familiarity with IND-enabling regulatory requirements and the nonclinical data package expected by FDA/EMA is a plus
- Experience evaluating potency, specificity, and developability trade-offs across vector, construct, or oligonucleotide candidates
- Strong scientific writing skills and ability to produce clear, evidence-supported rationale for drug development decisions
- Proficiency in AI agent use, with judgment to identify technically correct but pharmacologically or practically unsound reasoning
- Comfort operating in uncertainty and proactively flagging gaps in data or instructions
- Works with high agency and initiative
Benefits
Comp & perks- Health, dental, and vision insurance: 100% covered for the employee and 50% for dependents (US)
- 401(k) with no match (US)
- PTO: 12 days to start, increasing with promotions (US)
- Fully remote work option
- Onsite catered lunch and dinner and unlimited snacks
- Company outings most months
- Team off-sites
- Two career growth tracks: individual contributor and management
- OTE rises with each promotion
- First four weeks paid at full OTE during training
- Full OTE when quota cannot fairly apply
- Monthly advance of 60% of OTE for contractors outside the US, never clawed back
- H-1B, O-1, and TN visa sponsorship; STEM OPT support
- $10K sign-on if starting within 2 weeks of signing
- Equity offered