Nonclinical Documentation & AI-Driven Publishing Specialist

Scorpion Therapeutics; Pennsylvania; On-site; USD 95,000 - 135,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Medical/Dental/Vision

401(k) matching

Paid holidays

Vacation days

Sick/compassionate days

Job summary

Scorpion Therapeutics seeks a Nonclinical Drug Safety (NDS) Specialist in Information Management to coordinate, assemble, and manage regulatory documents for internal and external nonclinical studies. You will support Preclinical Development end-user operations in Veeva and help build internal processes to optimize document functions.

You will collaborate with NDS data scientists to establish a validatable generative AI pipeline for authoring/reviewing draft reports, and you will drive process

Qualifications

• BS/BA in relevant sciences with 3+ years relevant experience or MS/MA with 2+ years.
• Experience in nonclinical drug development programs (pharma/biotech).
• Advanced Veeva Vault operations (super/advanced user or equivalent) including process design/development and end-user support.
• Document lifecycle management (metadata, workflows, version control, records management).

Responsibilities

• Contribute to report automation using advanced document management to enable compliant, scalable generative-AI document generation for PCD.
• Build/implement/train processes and tools; act as Veeva super user/equivalent; troubleshoot issues; improve processes; support end-user training.
• Manage nonclinical study/document generation end-to-end using document management, publishing, and project planning tools.
• Facilitate quality review to ensure documents are accurate, complete, and consistent with regulatory/company expectations.
• Collaborate with internal/external stakeholders throughout document development.
• Develop/implement tools and metrics to improve processes and productivity.

Skills

APIs

Prompt engineering/LLMs

Systems thinking

Technical design/development

Document lifecycle management

Python

Education

BS/BA in relevant sciences

MS/MA in relevant sciences

Tools

Veeva Vault operations

Job description

Scorpion Therapeutics seeks a Nonclinical Drug Safety (NDS) Specialist in Information Management to coordinate, assemble, and manage regulatory documents for internal and external nonclinical studies. You will support Preclinical Development end-user operations in Veeva and help build internal processes to optimize document functions.

You will collaborate with NDS data scientists to establish a validatable generative AI pipeline for authoring/reviewing draft reports, and you will drive process