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Rhythm Pharmaceuticals

Federated Registry Data Scientist

Reposted One Month Ago
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In-Office
London, Greater London, England, GBR
Entry level
In-Office
London, Greater London, England, GBR
Entry level
Oversee the design and operation of a multi-country federated registry platform using OMOP CDM. Manage vendor deliverables, data collection, ETL, mapping, quality checks, analysis plans, cohort definitions, and federated query specifications. Assess research feasibility, review analytical outputs, support publications, resolve data issues with vendors and registry sites, and collaborate with scientific committees and internal stakeholders to generate real-world evidence.
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Company Overview
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 Overview
The 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 & Duties
  • Federated analyses
  • Oversee and supervise the vendor’s technical and analytical deliverables
  • Oversee data collection, data quality check, ETL logic and data mapping to OMOP CDM
  • Lead 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 internally
  • Perform external research proposals’ feasibility assessment before review by the Scientific Committee
  • Ensure analytical outputs are clear and consistent with research questions, develop report for review by the scientific committee, and support the drafting of related publications
  • Collaboration with vendors
  • Collaborate with the vendor on source data review, OMOP mapping, ETL logic, and data quality checks, helping to identify, prioritize, and resolve quality issues
  • Help with data-related questions raised by the vendor and coordinate timely responses from centers when local input is required
  • Ensure that data-related discussions remain aligned with Rhythm’s scientific objectives, project scope, timelines, and budget
  • Collaboration with sites/registries owners
  • Support sites in understanding project data requirements, minimum datasets, expected formats, timelines, and quality control processes
  • Coordinate 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 generation
  • Perform any other relevant tasks as needed to support the team and company objectives.
Qualifications & Skills
  • Advanced degree in Life Sciences, Data Science, Information Systems, or an equivalent scientific or technical discipline
  • Strong experience with healthcare data sources, including clinical registries, electronic health records, claims databases, healthcare databases, and real-world evidence projects
  • Strong proficiency in R and/or Python
  • Knowledge 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 results
  • Self-starter mentality who feels comfortable working in a fast-paced environment
  • Cross-functional mindset focused on a seamless collaboration with internal and external partners
  • Fluent in English
This role is home office based. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able travel internationally.
More about Rhythm
We 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 Are
We are committed to advancing scientific understanding to improve patients’ lives
We are inspired to tackle tough challenges and have the courage to ask bold questions
We are eager to learn and adapt
We believe collaboration and ownership are foundational for our success
We value the unique contribution each individual brings to furthering our mission
Inherent in our core values is the commitment to act ethically and with integrity in all we do.
 

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