[Hiring] Technical Staff Member - Regulatory Affairs/Medical Writer @Edison Scientific

Role Description

We are looking for a Forward-Deployed Regulatory Affairs/Medical Writer to join our Forward Deployed team. In this role, you will be working onsite with pharma and biotech partners alongside our engineers. You'll evaluate agent drafted content, build benchmarks to measure quality, and work with our partners' regulatory and medical writing teams to find where AI can meaningfully accelerate document preparation across the submission lifecycle. You bring the regulatory judgment that determines whether AI generated text is submission ready or needs rework.

This is embedded, partner facing work. You'll build credibility with regulatory and clinical teams, understand their writing conventions and agency expectations, and feed insights back to our AI team to improve how our platform reasons about regulatory content, structure, and scientific argumentation.

This position will ideally sit in San Francisco, Boston, or NYC; Remote is an option along with the ability to travel 20-40% of the time.

Responsibilities

• Evaluate and improve AI agent performance on regulatory and medical writing tasks including IND and NDA module drafting, clinical study reports, investigator brochures, briefing documents, and response to agency queries.
• Partner with end users at client organizations to validate that our AI generated regulatory documents meet the quality, accuracy, and compliance bar required for health authority submissions.
• Build benchmarks and acceptance criteria for regulatory writing focused agent workflows.
• Work directly with regulatory affairs professionals and medical writers at partner organizations to deploy AI agents into their document preparation workflows.
• Act as the regulatory content authority on AI generated outputs, assessing scientific accuracy, guideline compliance, internal consistency, and narrative quality.
• Collaborate daily with Forward Deployed Engineers on each account and support engagement scoping, success metrics, and technical evaluation with the Go-to-Market team.

Qualifications

• 5+ years of experience in Regulatory Affairs or Medical Writing within the pharmaceutical or biotechnology industry, ideally within a sponsor organization.
• Bachelor's degree required; advanced degree preferred (Ph.D., Pharm.D., M.D., or M.S. in a life sciences discipline).
• Strong understanding of regulatory requirements and familiarity with ICH guidelines and FDA/EMA expectations.
• Hands on experience authoring regulatory documents such as CTD module sections, clinical study reports, investigator brochures, and briefing documents, with exposure across IND through commercial submissions (NDA, BLA, MAA).
• Familiarity with eCTD structure and the end to end submission process from authoring through publishing.
• Experience in therapeutic areas such as oncology, immuno-oncology, immunology, cardiovascular, neurology, or hepatology (MASH) preferred.
• Experience with regulatory information management systems such as Veeva Vault or Documentum.
• Ability to travel 20-40% of the time.

Nice to Have

• Familiarity with AI assisted writing or document automation tools.
• High comfort with ambiguity and fast iteration.

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 off-sites and company events.