Tiger Analytics is pioneering what AI and analytics can do to solve some of the toughest problems faced by organizations globally. We develop bespoke solutions powered by data and technology for several Fortune 100 companies. We have offices in multiple cities across the US, UK, India, and Singapore, and a substantial remote global workforce. If you are passionate about working on business problems that can be solved using structured and unstructured data on a large scale, Tiger Analytics would like to talk to you. Responsibilities**Program Leadership & Delivery: **Lead the end-to-end delivery of complex data and analytics programs. Own the roadmap, from problem definition and solution design to production-grade deployment. **Stakeholder Management: **Act as the primary point of contact for client VPs and Directors. Translate unstructured business problems into high-level analytics solution designs. **Global Team Management**: Lead and mentor a hybrid team of onshore (US) and offshore (Global Delivery Center) data scientists and data engineers. Ensure seamless collaboration across time zones. **Solution Architecture:** Work with technical leads to design of scalable AI/ML pipelines and data architectures. Ensure solutions adhere to enterprise standards and leverage modern technology stack **Domain Expertise:** Apply deep Medical device domain knowledge to validate model outputs and ensure they align with industry nuances **Commercial Impact:** Present analytical findings and quantify the business value and drive the operationalization of AI into business processes.

Role Description Tiger Analytics is pioneering what AI and analytics can do to solve some of the toughest problems faced by organizations globally. We develop bespoke solutions powered by data and technology for several Fortune 100 companies. We have offices in multiple cities across the US, UK, India, and Singapore, and a substantial remote global workforce. If you are passionate about working on business problems that can be solved using structured and unstructured data on a large scale, Tiger Analytics would like to talk to you. - Program Leadership & Delivery: Lead the end-to-end delivery of complex data and analytics programs. Own the roadmap, from problem definition and solution design to production-grade deployment. - Stakeholder Management: Act as the primary point of contact for client VPs and Directors. Translate unstructured business problems into high-level analytics solution designs. - Global Team Management: Lead and mentor a hybrid team of onshore (US) and offshore (Global Delivery Center) data scientists and data engineers. Ensure seamless collaboration across time zones. - Solution Architecture: Work with technical leads to design scalable AI/ML pipelines and data architectures. Ensure solutions adhere to enterprise standards and leverage modern technology stack. - Domain Expertise: Apply deep Medical device domain knowledge to validate model outputs and ensure they align with industry nuances. - Commercial Impact: Present analytical findings and quantify the business value and drive the operationalization of AI into business processes. Qualifications - 13-15 years of total experience with 7+ years in Medical device domain with consulting. - Ability to engage with executive/VP level stakeholders from client’s team to translate business problems to high level analytics solution approach. - Deep knowledge and understanding of the Medical Device industry, including its unique commercial or operational landscape. - Strong project management and team management skills and ability to work with global teams. - Solid understanding of statistical and machine learning algorithms is a plus. - Strong SQL skills and experience with analytic tools like R & Python; & visualization tools like Qlik or Tableau is a plus. - Exposure to cloud platforms and big data systems such as Hadoop, HDFS, Hive is a plus. - Ability to work with IT and Data Engineering teams to help embed analytic outputs in business processes. - Graduate in Business Analytics or MBA or equivalent work experience. Benefits - Significant career development opportunities exist as the company grows. - The position offers a unique opportunity to be part of a small, fast-growing, challenging, and entrepreneurial environment, with a high degree of individual responsibility. Company Description Tiger Analytics provides equal employment opportunities to applicants and employees without regard to race, color, religion, age, sex, sexual orientation, gender identity/expression, pregnancy, national origin, ancestry, marital status, protected veteran status, disability status, or any other basis as protected by federal, state, or local law.

Role Description A Sr. Medical Science Liaison at Rapport is more than a scientific expert; they are a connector, collaborator, and trusted partner who helps bridge the external medical community with internal teams. By fostering trusted scientific relationships, generating meaningful insights, and supporting evidence development, the MSL helps shape Medical Affairs strategy while contributing to a team culture where people support one another, learn together, and celebrate shared success. Reporting to the Director, Field Medical, the MSL will support compliant scientific exchange, insight generation, evidence-related activities, and field execution aligned with Medical Affairs strategy. Your day-to-day: - Scientific Exchange & External Engagement - Build, maintain, and serve as a primary scientific contact for peer-to-peer relationships with scientific leaders, investigators, healthcare professionals, and academic centers within the assigned geography. - Conduct compliant, balanced, and evidence-based scientific exchange regarding disease-state science, clinical data, treatment paradigms, safety considerations, and the evolving competitive landscape. - Respond to unsolicited medical inquiries in accordance with company policies and applicable regulations, including inquiries related to clinical data, evidence interpretation, safety, and patient management considerations. - Represent Medical Affairs at medical conferences, scientific congresses, regional society meetings, and advocacy or educational events as appropriate. - Insight Generation & Communication - Gather, document, and synthesize field insights related to clinical practice trends, patient needs, barriers to care, emerging evidence, and competitive intelligence. - Communicate insights to appropriate internal stakeholders to inform medical strategy, evidence generation, scientific communications, lifecycle planning, and field execution. - Identify regional opportunities and challenges that may impact medical education, stakeholder engagement, evidence needs or launch readiness. - Education & Scientific Support - Deliver high-quality scientific presentations to healthcare providers, formulary or decision-making stakeholders, and internal teams, as appropriate. - Contribute to the development or review of scientific materials, including slide decks, FAQs, training resources, congress materials, advisory board content, and standard medical responses, when requested. - Support internal medical training and field readiness activities by sharing scientific expertise, field insights, and external stakeholder perspectives. - Cross-Functional Collaboration - Partner with Medical Affairs colleagues and cross-functional teams, including Medical Science, Clinical Trial Awareness, Regulatory, Safety, Market Access, Corporate Affairs, and Commercial, while maintaining strict compliance boundaries. - Provide scientific input and field perspective to support launch planning, competitive preparedness, medical education, payer-related scientific needs, and patient journey initiatives. - Escalate key scientific, safety, compliance, or reputational issues through appropriate internal channels in a timely manner. Qualifications - Advanced degree in a relevant scientific or clinical discipline required; PharmD, PhD, MD, DO, NP, or equivalent preferred depending on therapeutic area and business needs. - 5+ years of industry experience with at least 3 as an MSL with additional years in clinical, research, or related healthcare experience. - Epilepsy and/or neurology therapeutic area expertise and established network. - Strong understanding of clinical research, evidence generation, medical communications, and compliant scientific exchange. - Demonstrated ability to build credible peer-to-peer relationships with external scientific and clinical stakeholders. - Excellent written, verbal, and presentation skills, with the ability to tailor communication to diverse scientific and healthcare audiences. - Strong organizational skills and ability to manage a field territory, prioritize external engagements, and document insights in a timely manner. Requirements - Collaborative mindset: We are looking for individuals who are humble, curious, generous with their expertise, and committed to helping teammates succeed. We value collaboration over competition and seek people who elevate those around them. - Ability to travel approximately 50% or more depending on geography, business needs, and congress activity. Preferred - Prior experience in field medical affairs, medical communications, clinical development, real-world evidence, or investigator-initiated study support. - Psychiatry therapeutic area expertise. - Experience supporting pre-launch, launch, or post-launch medical activities. - Experience working in emerging biotech environment. Benefits - Every role has meaning. We’re determined to discover a better way for patients, and you’ll feel the passion from the start. - We are driven to innovate. Exciting science that pushes boundaries and opens new possibilities. - Your perspective matters. Stick your neck out, share your ideas – we work as a team. - We have FUN. We hire smart, dedicated, down-to-earth people that you’ll enjoy spending time with. - Leadership that CARES – about you, your growth + development. - We're bicoastal. Whether you're in the lab full-time in San Diego or taking advantage of a more hybrid work schedule in Boston – we make the most of our time together. - Competitive benefits. Including unlimited PTO, a lifestyle spending account, commuting reimbursement, and much more! - You get to be YOU! Show up as you are and make every day count. Your Compensation We get it. Compensation is an important part of your offer. You shouldn’t be surprised at the end of the recruiting process, and you should know that your offer is fair and equitable. How do we do this? We tell you about our hiring range now - we expect the hiring range for the role to be $180,000 to $200,000. Our actual offer will reflect a lot of factors including your relevant skills, experience, location, salary market data, and internal equity. In addition to a competitive salary, we also offer a pretty great benefits package. We don’t stop here - if you join Rapport, we go to the next level. We share our full salary ranges for every level across our company. Rapport Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.

• Build trust and credibility for Oura and our products for members, physicians, scientists and health systems. • Collaborate closely with engineering, product, design, data science and algorithm teams to define clinical features aligned with metabolic health, including integrations with continuous glucose monitors (CGM) and laboratory testing, and alignment with related teams such as sleep, activity and women’s health. • Collaborate on clinical feature specifications: Translate your metabolic health knowledge and existing literature into real-world informed performance goals, working closely with science and product teams. • Design and oversee clinical validation studies (feasibility, observational, real-world) to demonstrate product performance and clinical relevance in the metabolic space. • Work with regulatory, quality and clinical outcomes teams to build protocols, drive submissions and ensure compliance in applicable markets, and adapt to the changing regulatory environment in major markets. • Engage cross-functionally: proactively anticipate risks, communicate clearly about challenges, adjust plans, and maintain a collaborative mindset. • Serve as a clinical voice across the organization: staying abreast of the newest and most relevant medical insights, weaving this science into product decisions, translating this into company knowledge and features. • Guide the team on inclusion of appropriate biometrics and ground truth data, clinical endpoints, and study design. Uplevel internal knowledge across teams related to this domain of medicine and science. • Represent Oura externally to scientific audiences, payors, partners, clinicians and health systems.