• Develop research methods and data analysis plans related to healthcare utilization, cost trends, financial forecasting, member, and provider experience. • Expertly use appropriate software tools to retrieve, edit and tabulate data from various databases and files. • Conduct descriptive, prescriptive, predictive analyses. • Summarize complex data for leadership in the appropriate form (e.g., statistical summaries, narratives, charts, tables, graphs, etc.) to convey meaning, significance, and actionable information. • Contribute/Lead in the research and development of models, algorithms, and analysis tools to mature the use and creation of self-service data products at CareOregon. • Develop visual reporting (e.g., dashboards, scorecards, etc.) using data visualization tools such as Tableau when appropriate. • Develop appropriate subject matter, domain expertise and serve as an expert resource. • Collaborate with other subject matter experts to identify opportunities for building repeatable data products. • Collaborate with business teams to understand business needs and to illicit and document requirements for analytics, algorithms, models, etc. • Develop reporting tools to comply with regulatory reporting requirements. • Review and assess completeness, validity, and reliability of internal data used for analysis and reporting. • Create and maintain technical documentation such as data dictionaries, business glossaries, metric definitions, and other data resources. • Thoroughly document models, algorithms, data products, processes and any analysis, reports developed. • Contribute to, and actively participate in, community of practice to improve the skills and capabilities of other analysts at CareOregon. • Assist with, prepare, and/or deliver presentations to community groups, regulatory agencies, leadership, and other teams as needed.

Role Description We’re looking for a Senior Scientist, Study Toxicologist on the Nonclinical Safety team to help us expand what’s possible for patients with serious diseases. Reporting to the Associate Director, Toxicology Study Operations you’ll play a critical role in collaborating with project toxicologists and managing the outsourcing, design, and oversight of safety pharmacology and toxicology studies at contract research organizations (CROs). What You'll Do: - Collaborate with toxicology project leads and subject matter experts (e.g., discovery, bioanalysis, pharmacokinetics, CMC) to design safety pharmacology and toxicology studies, aligning with company objectives and regulatory standards. - Serve as the primary sponsor representative for CROs, handling all aspects of study outsourcing, including requesting quotes, negotiating contracts, and managing study timelines. - Oversee the design, execution, and data interpretation of nonclinical safety studies conducted at CROs, ensuring robust and high-quality data generation. - Review study reports and SEND datasets to ensure quality, timeliness, and readiness for regulatory submissions. - Effectively communicate study findings to toxicology project leads and senior management, addressing and resolving any study-related issues promptly. - Contribute to the preparation, review, and/or QC of nonclinical sections in regulatory submission documents (e.g., IBs, INDs, CTAs, NDAs, BLAs, MAAs, PIPs, Scientific Advice, annual reports, briefing documents) as needed. - Participate in issue-resolution teams, providing scientific guidance to address toxicology-related challenges and drive effective problem-solving. - Develop and enhance departmental SOPs and best practice documents to improve study operations and ensure regulatory compliance. Qualifications - You have a PhD or an MS and 3 years of toxicology experience or a BS and 5 years of toxicology experience in the pharmaceutical/biotechnology industry or at CROs. - Expertise overseeing safety pharmacology studies. - Proven track record of successfully directing and/or monitoring toxicology studies across various modalities, including small molecules, biologics, antisense oligonucleotides, and gene therapies. - Advanced knowledge of toxicology in support of drug development. - In-depth understanding of GLP regulations and regulatory guidance for nonclinical evaluations. Requirements - 5+ years of hands-on experience as a study director and/or monitor in toxicology (nice to have but not required). - Interest in expanding your experience with general toxicology studies. - Demonstrated enthusiasm for scientific research and a commitment to maintaining high-quality standards in toxicology study operations. - Strong strategic thinking, critical analysis, and leadership capabilities. - Self-motivated to meet performance objectives and to prioritize job-related tasks. - Ability to adapt to dynamic project needs and manage studies across different time zones. - Excellent interpersonal, communication, and negotiation skills, with a collaborative mindset. - Willingness and flexibility to travel on business to CROs. Benefits - Comprehensive medical, dental, and vision coverage and mental health support, annual wellbeing reimbursement, and access to our Employee Assistance Program (EAP). - Generous paid time off policies, fertility and family-forming benefits, caregiver support, and flexible work schedules with purposeful in-person collaboration. - 401(k) plan with a competitive company match, annual equity awards, and participation in our Employee Stock Purchase Plan (ESPP), and company-paid life and disability insurance. - Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities. - Employee resource groups, service and recognition programs, and meaningful opportunities to connect, volunteer, and give back. Company Description At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. That commitment has earned us recognition as Science magazine’s No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK.

• Work closely with CEO to help shape strategy and build data into all workflows • Own the data function end-to-end while leading a high-leverage team • Push what's possible with AI and help transform the company into a closed loop system • Build and ship AI tools, leading high-leverage investigations and audits

Role Description We're seeking a Senior Data Scientist focused on marketing analytics and advanced measurement—including methodologies like Marketing Mix Modeling, Attribution Models, and incrementality testing. Will be part of a global team, support markets across all regions, collaborating with consultants, analysts, and product leads. - Act as the technical referent for marketing measurement projects across global markets, guiding implementation within established frameworks. - Translate business needs into robust analytical solutions in collaboration with consultants and product teams. - Support the technical design, execution, and interpretation of models such as MMM, Advance digital Attribution models, and geo-lift tests. - Contribute to model deployment and integration into web-based platforms, in collaboration with product and data engineering teams. - Ensure consistency and quality across deliverables, promoting repeatable and privacy-first methodologies. - Represent technical capabilities in internal conversations and client-facing discussions. - Help maintain a knowledge-sharing culture across the team, and mentor junior team members when appropriate. Qualifications - A strong technical background, ideally with experience in statistics, econometrics, marketing analytics, or media measurement. - 3-5 years of experience working on analytics or measurement projects, with hands-on work in MMM, attribution, or experimentation. - Proficiency in Python (e.g., pandas, scikit-learn, statsmodels); SQL is required. - Familiarity with causal inference, time-series modeling, and regression analysis. - Experience working with media, CRM, or e-commerce datasets. - Excellent communication skills in English, both written and verbal. - Comfortable working in distributed, remote, and cross-functional teams. Requirements - Nice to Have: Experience with MMM libraries (e.g., Robyn, Meridian, LightweightMMM). - Exposure to cloud environments (e.g., GCP, BigQuery). - Understanding Martech ecosystem. - Bayesian background. Contract Type Permanent Company Description Here at Havas across the group we pride ourselves on being committed to offering equal opportunities to all potential employees and have zero tolerance for discrimination. We are an equal opportunity employer and welcome applicants irrespective of age, sex, race, ethnicity, disability and other factors that have no bearing on an individual’s ability to perform their job.