
Scientific Domain Expert
2 days ago
Job Description
In this vital role, you will work closely with research partners and technology peers to translate the technology and data needs for drug discovery research into technical requirements.
You will join a multi-functional team that implements LIMS platforms to capture, analyze, store, and report on pre-clinical and clinical studies. The ideal candidate will have deep scientific domain expertise and a passion for ensuring that technology solutions support data integrity and scientific workflows.
Roles & Responsibilities
- Requirements & Analysis: Function as a Scientific Business Systems Analyst within a Scaled Agile Framework (SAFe) product team. You will serve as a liaison between global Research Informatics and research scientists, translating complex scientific and technological needs into clear, actionable requirements, user stories, and supporting artifacts.
- Platform & Technology Management: Manage a suite of custom internal platforms, Commercial Off-the-Shelf (COTS) software, and system integrations. Lead the technology ecosystem for in vivo study data management and ensure that the platform meets the requirements for data analysis and data integrity.
- Product Roadmap & Risk Management: Develop and maintain a product roadmap that outlines planned features, enhancements, and timelines. Identify and manage technological and scientific validation risks associated with the systems.
- Compliance & Innovation: Ensure operational excellence, cybersecurity, and compliance. Scope scientific data operations into building Research-wide Artificial Intelligence/Machine Learning (AI/ML) capabilities.
- Collaboration & Support: Collaborate with geographically dispersed teams and foster a culture of collaboration, innovation, and continuous improvement.
Required Skills and Qualifications
- Proven expertise in a scientific domain area and related technology needs.
- Experience with writing user requirements and acceptance criteria in agile project management systems such as JIRA.
- Experience in configuration and administration of LIMS/ELN platforms (e.g., Benchling, Revvity, IDBS, STARLIMS, Watson, LabVantage).
- Experience using platforms such as Spotfire, Tableau, Power BI, etc., to build dashboards and reports.
- Experience handling GxP data and system validation, and knowledge of regulatory requirements (e.g., FDA 21 CFR Part 11, GLP, GCP).
- Knowledge of bioanalytical workflows and/or biospecimen management is a plus.
- Experience with cloud (e.g., AWS) and on-premise infrastructure is a plus.
- In-depth knowledge of Agile processes and principles for coordinated solutions and teams via SAFe.
Qualifications
- A Master's degree with relevant experience, a Bachelor's degree with extensive experience, or a Diploma with a substantial background in a Life Sciences, Computer Science, or a related field.
- Experience leading the implementation and supporting biopharma scientific software platforms is preferred.
- SAFe for Teams certification is preferred.
Benefits
- A challenging role with opportunities for professional growth and development.
- A collaborative and innovative work environment.
Others
- Please apply if you have a strong background in a scientific domain area and related technology needs.
- We look forward to hearing from you.
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