Federated Registry Data Scientist
Rhythm Pharmaceuticals Inc.
Company OverviewRhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases.
We develop medicines for previously untreatable or undertreated diseases.
We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need.
Their courage inspires us to challenge convention, ask bold questions and seek answers for them.
Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases.
We develop medicines for previously untreatable or undertreated diseases.
We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need.
Their courage inspires us to challenge convention, ask bold questions and seek answers for them.
Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.Opportunity OverviewThe Federated Registry Data scientist will contribute to the design, development and operation of a multi-country federated registry platform based on the Observational Medical Outcomes Partnership Common Data Model (OMOP CDM), in collaboration with specialized vendors for Extract-Transform-Load (ETL), hosting, and federated analyses.The role will serve as a primary point of contact between Rhythm, the selected vendors, and participating registries for data-related activities.
The Data Scientist will oversee the local registry data collection (mapping, transformation, quality-check) and the federated analyses specifications and outputs within a federated OMOP CDM-based environment provided and maintained by the vendors.Responsibilities & DutiesFederated analysesOversee and supervise the vendor's technical and analytical deliverablesOversee data collection, data quality check, ETL logic and data mapping to OMOP CDMLead preparation and review of the statistical analysis plan, cohort definitions, variable definitions, and federated query specifications supported and executed by the vendors based on research questions proposed by the Scientific Committee, the participating centers or internallyPerform external research proposals' feasibility assessment before review by the Scientific CommitteeEnsure analytical outputs are clear and consistent with research questions, develop report for review by the scientific committee, and support the drafting of related publicationsCollaboration with vendorsCollaborate with the vendor on source data review, OMOP mapping, ETL logic, and data quality checks, helping to identify, prioritize, and resolve quality issuesHelp with data-related questions raised by the vendor and coordinate timely responses from centers when local input is requiredEnsure that data-related discussions remain aligned with Rhythm's scientific objectives, project scope, timelines, and budgetCollaboration with sites/registries ownersSupport sites in understanding project data requirements, minimum datasets, expected formats, timelines, and quality control processesCoordinate with sites and the vendor to investigate data quality issues such as missing data, inconsistent values, duplicate records, etc.Collaborate with research teams (scientific committees, internal stakeholders, participating sites) to develop insights and drive evidence generationPerform any other relevant tasks as needed to support the team and company objectives.Qualifications & SkillsAdvanced degree in Life Sciences, Data Science, Information Systems, or an equivalent scientific or technical disciplineStrong experience with healthcare data sources, including clinical registries, electronic health records, claims databases, healthcare databases, and real-world evidence projectsStrong proficiency in R and/or PythonKnowledge of healthcare standards, including OMOP CDM, Fast Health Interoperability Resources (FHIR), Systemized Nomenclature of Medicine Clinical Terms (SNOMED CT), etc.Knowledge of statistical methods in real-world evidence (RWE)Strong communication and interpersonal skills, capable of engaging with senior leadership and key stakeholders.Not accepting the status quo, working with a sense of urgency to deliver resultsSelf-starter mentality who feels comfortable working in a fast-paced environmentCross-functional mindset focused on a seamless collaboration with internal and external partnersFluent in EnglishThis role is home office based.Rhythm operates in a hybrid-work model.
Candidates applying must be willing and able travel internationally.More about RhythmWe are a dynamic and growing global team spanning more than a dozen countries.
At Rhythm we are dedicated to transforming the lives of patients living with rare melanocortin-4 receptor (MC4R) pathway diseases by rapidly advancing care and precision medicines that address the root cause.
Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.At Rhythm Our Core Values AreWe are committed to advancing scientific understanding to improve patients' livesWe are inspired to tackle tough challenges and have the courage to ask bold questionsWe are eager to learn and adaptWe believe collaboration and ownership are foundational for our successWe value the unique contribution each individual brings to furthering our missionInherent in our core values is the commitment to act ethically and with integrity in all we do.
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