Role Description Thrivable is a real-time healthcare market research platform helping patients, pharmaceutical companies, and medtech organizations develop better products, services, and experiences through fast, actionable patient insights. We're looking for a hands-on researcher who excels at the technical and creative process of pulling together patient survey data into coherent, compelling narratives. This role is about creating survey instruments and digging into the data to find the story that matters for our clients. This is not a “manage from a distance” role. We need someone who is willing to do the actual work — programming surveys, digging through messy data, reviewing transcripts, synthesizing findings, building decks, and delivering strategic recommendations. The right person is both intellectually sharp and execution-oriented. This role is ideal for someone coming from academic research, healthcare research, consulting, agency work, or a postdoctoral environment who wants broader ownership and faster-moving work. What You'll Do - Synthesize complex research data into clear, coherent, and visually compelling narratives for pharmaceutical and medtech clients. - Deliver research findings to clients with a focus on actionable insights, ensuring all data is translated into meaningful business implications. - Design and execute quantitative and qualitative healthcare research studies. - Program and troubleshoot surveys in Qualtrics. - Analyze quantitative data using Qualtrics analytics, SPSS, R, Python, or similar tools. - Apply statistical thinking to identify meaningful patterns, trends, and implications in complex datasets. - Conduct qualitative coding, synthesis, and insight development. - Translate findings into clear business, patient, and healthcare implications. - Build executive-level reports and presentations. - Present findings to clients and contribute to strategic discussions. - Use AI tools thoughtfully to improve research workflows while understanding their limitations, risks, and appropriate applications. - Support pharmaceutical, medtech, and broader healthcare research initiatives across therapeutic areas. Qualifications - Exceptional data storytelling skills, with the ability to turn survey results into a structured and persuasive narrative. - Strong quantitative and qualitative research skills, including research interview moderation. - Strong statistical analysis skills and comfort working directly with data. - Healthcare experience, education, or research background. - Experience presenting research findings directly to stakeholders or research sponsors. - Proficiency in statistical analysis tools (SPSS, R, Python, SAS) to validate the data behind your insights. - Experience with Qualtrics survey programming and/or Qualtrics-based analytics strongly preferred. - Proficiency in Microsoft Office and Google Workspace, especially PowerPoint/Slides and Excel/Sheets. - Strong communication, storytelling, and presentation skills. - Comfort using AI tools to improve research efficiency and workflows, with strong judgment around data privacy, hallucinations, bias, source validation, and appropriate use cases. - Ability to work independently in a lean, high-accountability environment. - Willingness to be highly hands-on across all aspects of research execution. Requirements - Diabetes expertise or endocrinology experience. - Experience in healthcare market research, pharma, biotech, medtech, or agency environments. - Proven experience in a research-heavy role where you were responsible for the final delivery of insights and findings, bonus for this to be client facing consulting or agency role. - Mixed-method research experience. - Experience moderating interviews or conducting qualitative synthesis. - Familiarity with clinical development or clinical trial research. Education - Advanced degree preferred (PhD, MPH, MS, etc.), but we will absolutely consider candidates with a bachelor's degree and strong relevant experience. Benefits - Fully remote. - High ownership and visibility. - Opportunity to shape meaningful healthcare research. - Small, fast-moving, collaborative.

• Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard. • Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality. • Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations. • Review CRFs (electronic or paper) and subject source documentation for validity and accuracy. • Verify proper management and accountability of Investigational Product. • Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate. • Monitoring Close-out visits in Ukraine.

• Contributes to Child Care Aware® of America’s research projects to analyze and benchmark state child care standards. • Participates in data collection and analysis, utilizing multiple research methods as needed (e.g., surveys, questionnaires, case study methods, interviews, etc.) • Communicates and translates data into research products that are easily understood and digested by system leaders, policymakers and CCAoA partners. • Maintains data and associated databases for key research reports. • Develops and maintains relationships with external stakeholders, particularly those who provide data for CCAoA analyses, regularly interfacing with them regarding research requests. • Partners with colleagues and other CCAoA units to execute projects in support of Research Team goals. • Performs other related duties as required and assigned.

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans. • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. • Demonstrates diligence in protecting the confidentiality of each subject/patient. • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. • Assesses site processes according to the Clinical Monitoring/Site Management Plan (CMP/SMP). • Conducts Source Document Review of appropriate site source documents and medical records. • Verifies required clinical data entered in the case report form (CRF) is accurate and complete. • Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. • Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. • Verifies site compliance with electronic data capture requirements. • May perform investigational product (IP) inventory, reconciliation and reviews storage and security. • Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. • Verifies issues or risks associated with blinded or randomized information related to IP. • Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned. • Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. • Reconciles contents of the ISF with the Trial Master File (TMF). • Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. • Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. • Supports subject/patient recruitment, retention and awareness strategies. • Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. • For assigned activities, understands project scope, budgets, and timelines; manages site-level activities/communication to ensure project objectives, deliverables and timelines are met. • Must be able to quickly adapt to changing priorities to achieve goals/targets. • May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. • Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. • Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. • Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. • Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.