• Deliver comprehensive data management services across all study phases • Independently own assigned data management studies and deliverables from startup through database lock, proactively identifying risks, resolving issues, communicating status, and escalating when appropriate • Ensure clinical databases are complete, accurate, and compliant with Sponsor and regulatory standards • Serve as primary Sponsor contact for data management activities • Lead data management communications and coordinate with internal and external teams to ensure timely delivery of study milestones and progress updates • Train site staff (CRCs, CRAs, PIs) and client teams on EDC systems • Oversee CRF lifecycle from design to final delivery • Conduct User Acceptance Testing (UAT) and ensure database setup aligns with specifications • Develop and manage essential study documents (e.g., Data Management Plan, CRF Completion Guidelines, Validation Plans, SAE Reconciliation Plans) • Review and clean clinical data, manage queries, and reconcile third-party data • Coordinate database lock and final data delivery • Identify risks and proactively resolve project issues • Provide exceptional service to internal and external stakeholders

• Partner with Product, Engineering, Design, and Operations to inform and shape product strategy, prioritization, and decision-making • Develop metrics, data models, and analytical frameworks that improve how teams understand customer behaviour and business performance • Identify opportunities to improve customer experience, growth, retention, and operational efficiency through data • Translate complex business questions into clear recommendations and actionable insights • Proactively surface trends, risks, and opportunities that help the team focus on the highest-impact work • Collaborate with Analytics Engineering to improve the quality, scalability, and usability of data foundations for the team

Role Description Terray Therapeutics is seeking a highly motivated and experienced in vivo scientist with expertise in models of autoimmunity and inflammation to join our Translational Biology team. In this role, the candidate will serve as a scientific and operational lead for outsourced in vivo pharmacology and nonclinical safety/toxicology studies, with responsibilities including study design, execution and monitoring, vendor oversight, project management and cross-functional coordination. The position will report to the Director of Translational Biology. - Provide scientific leadership and oversight for in vivo pharmacology studies focused on inflammation, autoimmunity, or related therapeutic areas in support of advancing our pipeline programs. - As the pharmacology representative, collaborate cross-functionally with preclinical teams, project leads, and external consultants to advance our pipeline programs through in vivo studies. - Lead and monitor outsourced in vivo pharmacology and nonclinical safety/toxicity studies conducted at CROs, ensuring scientific rigor, protocol compliance, data quality, and timely execution. - Contribute to study design, protocol development and review, endpoint selection and data interpretation. - Review study reports, datasets and summaries to ensure scientific accuracy and completeness. - Coordinate study timelines, logistics, milestones, budgets and deliverables across multiple external vendors and internal stakeholders. - Manage CRO relationships, including vendor selection, performance oversight, issue resolution and communication. - Maintain study documentation, ensuring compliance with regulatory requirements and company policies. - Present study updates and recommendations to project teams and leads. - Support contract management activities (scopes of work, purchase orders, invoice tracking). Qualifications - Ph.D. degree in biology, immunology, pharmacology, toxicology, or a related field. - 3+ years of experience in biotech or pharmaceutical industry supporting nonclinical drug development programs. - Strong scientific background in inflammation, immunology, or immune-related diseases. - Extensive experience with rodent in vivo pharmacology and translational disease models. - Strong scientific data analysis, interpretation, and problem-solving skills. - Strong understanding of nonclinical drug development workflow. - Experience managing or monitoring outsourced studies at CROs. - Demonstrated project management and organizational skills with the ability to manage multiple studies and priorities simultaneously. - Excellent written, verbal, and presentation skills. - Ability to work effectively in cross-functional teams and to thrive in a highly collaborative research environment. Requirements - Experience with vendor oversight, contract management, and budget tracking. - Experience supporting IND-enabling and preclinical development programs. - Knowledge of GLP and non-GLP study conduct and non-clinical assessment. - Familiarity with IACUC regulations and animal welfare standards. Benefits - Compensation: $120,000 – $175,000 annually, depending on experience. - Participation in the Company’s stock option plan. - 3% retirement safe harbor contribution. - Fully paid health, dental, vision insurance for employees, spouses, partners, and families. - Above-market life insurance and disability coverage. - Additional benefits to explore during the offer process.

• Build AI-assisted workflows and internal tooling • Prototype and productionize LLM-enabled applications • Develop scalable analytics and decision-support systems • Improve self-service data access safely and responsibly • Reduce operational burden through automation and intelligent systems • Help evolve internal governance and semantic consistency practices