Associate General Counsel – Regulatory and Technology
Pathos · United States · US
Regulatory Affairs
Remote
Not yet analysed
Demand80
Career growth85
Healthcare fit35
Remote potential50
5-year outlook
Strong for experienced regulatory and legal counsel in AI-driven biotech, but compensation depends on bar admission, location, equity, and FDA/technology experience. Exact figures are not provided.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-07
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Only lawyers with FDA drug development and technology experience should apply; clinicians without legal credentials are unlikely to qualify. However, it is a strong signal of AI and regulatory demand in oncology.
Who should apply
Attorneys with FDA drug development law, privacy, compliance, and AI/software experience; MD/JD or PharmD/JD professionals with oncology or regulatory backgrounds.
CV angle
If you have legal training plus clinical experience, frame oncology trial knowledge, FDA interactions, privacy/compliance, AI governance, and cross-functional work with engineering and product teams. Do not fabricate legal credentials.
Skills to highlight
- FDA drug development law
- Regulatory strategy
- Privacy compliance
- AI governance
- Corporate compliance
- Oncology clinical trials
- Cross-functional collaboration
- Risk management
Role summary
Legal counsel role advising engineering, product, and clinical teams on FDA drug development law, privacy, compliance, and AI guidelines for oncology AI platforms and clinical-stage programs.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.