Clinical Informaticist
$119k - $179kVerily
Clinical Pharmacy InformaticistVerily Health is a data platform and technology company purpose-built to power AI-enabled precision health solutions that accelerate research and improve care for individuals and communities. Uniquely positioned at the intersection of technology, data science, and healthcare, Verily transforms multimodal health data into insights, models, and actions that make healthcare more personalized, predictive, and precise.ResponsibilitiesArchitect FHIR-compliant data models, ensuring all instantiated resources align with specific implementation guides (IGs), profiles, and internal architectural standards.Design and operationalize sophisticated data harmonization and enrichment strategies to unify disparate data streams from EHRs, HIEs, and claims sources.Act as the subject matter expert for clinical ontologies (SNOMED CT, LOINC, ICD-10, RxNorm); define and maintain custom value sets to support specialized clinical use cases.Establish rigorous validation frameworks and automated rules to ensure the clinical accuracy, consistency, and longitudinal integrity of our data assets.Develop clear and concise documentation that effectively communicates data design requirements to engineering teams and stakeholders with varying levels of technical expertise.QualificationsBachelor's Degree in Computer Science, Information Systems, or a closely related technical degree.Professional Certificate or Master's Degree in Clinical Informatics or equivalent professional experience in a clinical informatics role.Minimum of 5 years experience working in clinical informatics or data integration in Healthcare or Life Sciences industriesDemonstrated proficiency in navigating the complexities of interoperability standards and frameworks (HL7 v2, FHIR CDA/CCD-A, NCPDP) and data models (FHIR R4/R5, OMOP).Advanced proficiency in Python and SQL.Preferred QualificationsHands-on experience with dbt (data build tool), Jupyter Notebooks, and Experience in healthcare data integration.Excellent communication and interpersonal skills.Ability to work independently and as part of a team.Qualified applicants must not require employer sponsored work authorization now or in the future for employment in the United States.The US base salary range for this full-time position is $119,000 - $179,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.Verily Health Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here. If you'd like more information on your EEO rights under the law, please click here.If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.
- Analysis Group, Inc. is hiring a Biostatistician in Boston to support clinical trial analysis and decision-making. The successful candidate will apply biostatistical methods and manage analyst teams, with responsibilities in regulatory submissions and data integration....Suggested
- ...management, and regulatory submissions. This role focuses on statistical design, analysis, and CDISC-compliant reporting for diverse clinical trials. The candidate will lead SAS programming efforts, collaborate with protocol design teams, and guide junior staff while...Suggested
- ...communication skills as you guide study design, analyses, and reporting. The candidate should have a Master’s in biostatistics and at least 20 years of experience, with proficiency in SAS and R and a track record in clinical trials research. #J-18808-Ljbffr Frontier ScienceSuggested
$94k - $128k
Job Summary The Senior Clinical Data Analyst independently executes assigned clinical studies activities, applying comprehensive scientific knowledge to clinical data collection, management, quality assessment, analysis support, and documentation. This fully qualified...SuggestedWork experience placementWork at officeLocal areaRemote work$80k - $115k
...employees, and communities.The RoleAs a Senior Healthcare Data Informaticist, you will design, manage, and maintain all reference data assets in the Terminology Reference Library (TRL), including clinical, and claims-related coding standards. In this senior role, you will...SuggestedWork at officeLocal areaWork from home$203k - $247k
...Principal BiostatisticianBoston, MAThe OrganizationWhat's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that...Work at officeLocal areaRemote work$123k - $163k
...biostatistician on multiple projects. With your keen analytical skills, you will perform statistical analyses, interpret results, and prepare clinical study reports, including integrated summaries for submissions. Your role will also involve reviewing analyses performed by other...Temporary workLocal areaWorldwide- ...statisticians to carry out all statistical tasks and responsibilities within a wide range of collaborative research studies, including clinical trials, varying from small phase 1 to large phase 3 studies across many different study designs and disease areas. A great degree...Interim roleWork at office
$145k - $179k
...quantitative expertise to support the development, validation, and regulatory submission of FMI's comprehensive genomic tests; to generate clinical evidence for FMI's innovative assays by designing and executing statistical analysis plans; and to solve scientific problems by...$152k - $228k
...drug developer mindset. Key Duties and Responsibilities: Conducts advanced scientific and operational statistical work for multiple clinical trials, observational studies, or real world data (RWD) investigations, including the design, development and execution of the...Summer workRemote workFlexible hours2 days per week$60k - $99k
...Division and CardioVascular Institute is seeking a highly motivated individual with expertise in biostatistics to work on multiple clinical and translational research projects focused on cardiovascular disease. This Biostatistician position offers the opportunity to...TraineeshipWork experience placement$178k - $216k
...Salary Range: $178,000.00 To $216,000.00 Annually PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. We’re driven by our passion for...Work experience placement$195k - $255k
...Biostatistician PositionAnalysis Group is seeking an experienced professional to support the continued growth of our clinical trial and biostatistics capabilities. This role is suited for candidates with a strong foundation in clinical trial data, statistical programming...Work experience placementWork at officeLocal areaVisa sponsorship$210k - $255k
...on health care. Analysis Group’s health care experts apply analytical expertise in health economics and outcomes research (HEOR), clinical research, market access and commercial strategy, health care policy, epidemiology and drug safety, data science, and biostatistics...Work experience placementWork at officeLocal areaVisa sponsorship- ...Entrada Therapeutics is seeking a Senior Biostatistician to lead daily statistical activities for multiple clinical programs in a part-time capacity (~20 hours per week). Reporting to the Head of Biometrics, you will shape statistical approaches for trials and supervise...Part time
$132.2k - $198.2k
...Responsibilities Within assigned area, designs, develops and executes the technical/statistical infrastructure for the conduct and evaluation of clinical trials, observational studies, or real world data (RWD) investigations, including related areas/activities. Participates in...Summer workRemote workFlexible hours2 days per week$75k - $80k
...in both written and oral formats to drug and device manufacturers, and doctors. The statistical analyses vary across patient-level clinical trial data, observational study (real-world) data, and published aggregate data. Our work involves a range of techniques such as...Permanent employmentFull timeTemporary workWork at officeWork from homeFlexible hours$80k - $115k
..., and communities. The Role As a Senior Healthcare Data Informaticist, you will design, manage, and maintain all reference data assets in the Terminology Reference Library (TRL), including clinical, and claims-related coding standards. In this senior role, you will...Work at officeLocal areaRemote workWork from homeFlexible hours3 days per week$116k - $151k
...collaborate with cross-functional teams composed of internal and/or external experts. Responsibilities: Provide statistical support to clinical studies or projects under the guidance of senior Biostatistics leadership. Collaborate with cross-functional teams in support of...Temporary workRemote work$72.8k
Overview The Healthcare Data Analyst will join a collaborative team at Joslin Diabetes Center supporting clinical operations, grounded in patient safety and improvement science to participate in projects that promote a culture of excellence. The Healthcare Data Analyst...Work experience placement- ...Our client, a biotechnology company, is seeking a Biostatistician to support ongoing clinical trial programs from their Boston office. This contract role involves designing statistical analysis plans, analyzing clinical trial data, and producing reports that support regulatory...Hourly payWeekly payPermanent employmentContract workTemporary workWork at office
$250k - $330k
...providing patient care, this physician has dedicated time as a clinician informaticist, reporting to the CHIO. Highlights Physicians will work in various settings including at one of our three outpatient clinics, inpatient on Labor & Delivery, and in the operating room....Full time$250k - $330k
...providing patient care, this physician has dedicated time as a clinician informaticist, reporting to the CHIO.Highlights:Physicians will work in various settings including at one of our three outpatient clinics, inpatient on Labor & Delivery, and in the operating room....Full timeLocal areaWork from home$75k - $80k
...in both written and oral formats to drug and device manufacturers, and doctors. The statistical analyses vary across patient‑level clinical trial data, observational study (real‑world) data, and published aggregate data. Our work involves a range of techniques such as...Permanent employmentFull timeWork at officeFlexible hours- Population Health Informaticist (AI Training) We're partnering with the world's leading AI research teams to build smarter, more accurate... ...Familiarity with public health surveillance frameworks or clinical data standards (e.g., ICD codes, HL7, FHIR) Why Join Us Work...Hourly payOngoing contractContract workRemote workFlexible hours
$110k
...researchers, doctors, and policymakers make informed decisions. Biostatisticians play a pivotal role in advancing medical research, clinical trials, epidemiology, and public health by extracting meaningful insights from data. 2. Roles and Responsibilities As a...Work at officeWorldwide- ...issues Make decisions at the study level across various studies, leading and prioritizing tasks globally Collaborate closely with clinical research, regulatory affairs, CROs, Commercial, Worldwide Medical, KOLs, and other disciplines Monitor needs and determine...Worldwide
$119.7k - $222.3k
...study or project level, and you will be responsible for all statistical work, scientific and operational, in collaboration with the clinical trial teams and other quantitative partners in the Early Development - Advanced Quantitative Science's team. Job Description Your...Relocation package- Job-ID32188507Reference26-00483 Job Description: Design, build, and configure clinical study databases in EDC/CDM platforms. Ensure systems meet client needs, follow GCDMP, support accurate data capture, workflows, edit checks, and integrations. Responsibilities: Lead...Remote work
- ...organization within the Harvard T.H. Chan School of Public Health, is responsible for the design, monitoring and statistical analysis of clinical trials and observational studies for several major national and international NIH-funded clinical research networks. CBAR employs...Remote work
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