The EMMES Corporation

Overview: Job Posting Title India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose We are hiring a Product Owner with 5–8 years of experience to help define, prioritize, and deliver AI-powered authoring solutions for clinical trial documentation. You will support the development of the Veridix Authoring Agent, a GenAI product that accelerates the creation of clinical documents like protocols, SAPs, CSRs, and safety reports. This role serves as a key liaison between product management, engineering, clinical experts, and AI teams to ensure delivery of compliant, usable, and high-impact authoring tools for sponsors and internal teams. The ideal candidate will have experience working on AI-driven or data-centric healthcare applications, a deep understanding of agile product practices, and a strong interest in transforming clinical trial operations with generative AI technologies. Responsibilities: Own and manage the product backlog for AI-driven clinical trial document authoring capabilities, including document drafting, review workflows, and expansion across document types. Translate product and clinical requirements into detailed epics, user stories, and testable acceptance criteria. Collaborate with engineering, AI/ML teams, QA, and clinical SMEs to deliver validated features in fast, iterative releases. Drive agile ceremonies such as backlog refinement, sprint planning, and retrospectives in coordination with scrum master and cross-functional teams. Ensure authoring solutions support compliance with regulatory standards (e.g., GCP, 21 CFR Part 11, HIPAA) and audit-readiness. Validate feature priorities with product managers, clinical users, and internal experts across domains (medical writing, biostatistics, regulatory). Help define and track product KPIs such as draft quality, turnaround time, and user adoption. Coordinate user acceptance testing (UAT), support training materials, and ensure proper documentation of releases. Contribute to long-term product strategy and roadmap for AI-enabled authoring workflows and modular document automation. Qualifications: Bachelor’s or Master’s degree in Life Sciences, Engineering, Computer Science, or a related field. 8-10 years of experience as a product owner or product manager in clinical research, digital health, or healthcare SaaS. Ability to work with UX/UI designers, backend/frontend engineers, data scientists, SQA and Product Managers. Strong understanding of agile development processes, Jira-based workflows, and product lifecycle best practices. Experience writing user stories and managing end-to-end sprint execution with cross-functional teams. Exposure to AI/ML or LLM-based technologies, especially for content generation or automation, is a strong plus. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes #LI-Remote