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Statistician
As a distributed company with no single brick and mortar office, Lantana can hire the best available talent and offer a flexible work schedule. The ability to travel to the annual Lantana Retreat and occasional client meetings is preferred. Lantana Consulting Group provides services and software for standards-based health information exchange. The statistician will contribute to the wider Lantana team's success by supporting analytics as needed and contributing to proposals, as needed, as they relate to quantitative analyses. $83k-117k yearly est.7d agoSenior Biostatistician, FSP (Remote)
We are seeking Senior Biostatistician to lead large global or other major projects, analyze all parts of any clinical study, and provide planning on multiple clinical studies from multiple clients including tracking project activities and project time management. - Perform Lead Biostatistician role on medium complexity studies, providing statistical oversight and attending relevant project meetings Senior Biostatistician, FSP (Remote) These permanent, remote opportunities can be worked from anywhere in U. S. or Canada. $115k-145k yearly8d agoSenior Statistician - Epidemiology & Scientific Affairs
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. The Senior Statistician provides statistical and programming expertise to the ESA Team through leadership in representing ESA statistical services, collaborations with other statistical teams across the organization, and project delivery, including Clinical Data Interchange Standards Consortium (CDISC) SDTM/ADaM standards as necessary, leading-development activities, business initiatives and long-term planning. When needed, the Senior Statistician will provide statistical as well as programming expertise. $86k-109k yearly est.28d agoBiostatistician - Epidemiology/Clinical Research - REMOTE
Westat is seeking a Biostatistician to support statistical analyses on various types of research projects involving epidemiological, administrative, and clinical datasets. Westat's research, technical, and administrative staff of more than 2,000 is located at our headquarters in Rockville, Maryland, near Washington, DC. Westat is committed to building a diverse workforce and a culture of inclusivity, belonging and equity for all. Westat is an employee-owned corporation providing research services to agencies of the U.S. Government, as well as businesses, foundations, and state and local governments. You will provide biostatistical support including designing analytic plans and performing data analysis for Westat projects and contribute to scientific peer reviewed publications. $97k-126k yearly est.9d agoBiostatistician - PhD Remote (Full-time or Part-time)
The Biostatistician develops systems for monitoring the quality of clinical data. The Biostatistician maintains expertise in state-of-the-art data manipulation and statistical methodology. Emmes complies with all applicable laws regarding reasonable accommodations or The Emmes Company, LLC ("Emmes") is a global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public health and biopharmaceutical innovation. We believe in the power of truth, so much so that we named our company Emmes, which means truth. You will be joining a collaborative culture that empowers every Emmes employee - from entry level through top executive - to contribute to our clients' success by sharing ideas openly and honestly. Emmes only requires all US new hires in the following job categories to be fully vaccinated before their first day of employment: (i) Clinical Research Associates (CRAs), (ii) Associate CRAs, and (iii) all CRA line managers. The Biostatistician ensures high-quality statistical support is provided for clinical trials, registries and basic research using advanced statistical skills and knowledge of clinical research. The Biostatistician collaborates with clinical investigators to determine study design, contributes to protocol development, writes statistical analysis plans, performs statistical analysis and inference and writes and presents reports summarizing findings including publications in peer-reviewed journals. $76k-104k yearly est.49d agoSenior Biostatistician - Remote
The Senior Biostatistician serves a lead role on projects. ClinChoice is a global CRO supporting data management, biostatistics, statistical programming, clinical operations, regulatory affairs, safety, pharmacovigilance, toxicology, medical affairs, medical writing, quality, risk, and compliance services to the pharmaceutical, biotechnology, and medical device industries worldwide. ClinChoice was established in the US in 1995, and has grown to more than 3,000 employees worldwide, with key offices and delivery centers in the US, UK, China, India, Armenia, Japan and throughout the Asia-Pacific region. $75k-106k yearly est.56d agoStatistician Analyst
The Statistician Analyst will support the US Department of State in decision-making by collecting, analyzing, and presenting data. Learn more about what working at Chenega MIOS can mean for you. At Chenega MIOS, our professional development plan focuses on helping our team members at every level of their careers to identify and use their strengths to do their best work every day. If so, Chenega Military, Intelligence & Operations Support (MIOS) could be the place for you! The Statistician Analyst may work in a variety of files and use their mathematical skills to understand data trends before presenting reports to business managers and stakeholders. $73k-102k yearly est.21d agoMid. Statistician Mathematician
Prescient Edge is seeking a Mid. Statistician/ Mathematician to support a federal government client. Benefits: At Prescient Edge, we believe that acting with integrity and serving our employees is the key to everyone's success. Prescient Edge is a Veteran-Owned Small Business (VOSB) founded as a counterintelligence (CI) and Human Intelligence (HUMINT) company in 2008. $73k-104k yearly est.48d agoStatistician - Senior
Job DescriptionWe are seeking a Sr. Statistician to join our growing team supporting a federal surveys program located in the Washington DC metropolitan area. This position is contingent upon contract award. Responsibilities: * Oversees the administration of priority statistical collections. * Uses subject-matter expertise for data collection methodology (including surveys) and data analysis and presentation to develop, execute, and report on studies. * Serves as a key technical consultant to other federal customer components seeking to improve their collection, analysis, and reporting of data. * Conducts research on methodological issues in measuring biases in data from various subpopulation groups. * Designs and executes a program of original in-depth studies that apply quantitative analysis and sophisticated statistical techniques to data collected. * Conducts strategic planning with respect to survey design, analytic direction, and workload management. Position Requirements : * 8 years of experience as a Statistician designing sampling plans and performing the weighting of complex surveys. * Advanced degree in Statistics, Mathematics, Data Science, Engineering, Computer Science, Information Technology, or related field. Ph.D. preferred. * Must provide one example of a complex sampling plan and one example of a complex weighting plan to be considered. Clearance Requirments: * Must be able to attain and retain a Public Trust Clearance. Synectics is an Equal Opportunity Employer. $72k-96k yearly est.36d agoSenior Statistician
KBR is seeking a Statistician to support government customers in the Washington Metropolitan Area. $68k-101k yearly est.27d agoSenior Statistician
The Senior Statistician will leverage experience and expertise in running complex statistical models involving large data sets to inform the interpretation, analysis, synthesis and reporting of these data. Job DescriptionSenior Statistician, PHCoE Prometheus Federal Services (PFS), is seeking a Senior Statistician to join our growing team supporting The Psychological Health Center of Excellence (PHCoE) within the Defense Health Agency (DHA) in the Washington, DC Metro Area. The Senior Statistician will have a PhD and five or more years of post-doctoral experience analyzing and modeling health-related research data. $70k-102k yearly est.27d agoOncology Data Spec II
Role: Oncology Data Specialist II 1. Aligns all work and resource management with Health Catalyst's mission, cultural attributes and operating principles. Over the years, Health Catalyst has achieved and documented clinical, operational, and financial improvements for many of the nation's leading healthcare organizations. Maintains aspects of the Oncology Data Registry (Cancer Registry) according to state law, the Commission on Cancer (COC), American College of Surgeons, all regulatory standards and reporting guidelines. $50k-76k yearly est.6d agoClinical Documentation Specialist (Remote Work) - Clinical Data Management
**Galveston, Texas, United States** Medical Administrative UTMB Health Requisition # 2302012 **Minimum Qualifications:** + Certified Registered Health Information Administrator (RHIA), or Technician (RHIT), or an associate degree in a health care related discipline with Certified Coding Specialist (CCS) certification, and a minimum of 3 years medical coding experience. **Or** + Registered nurse (or medical school graduate) with a minimum of 3 years inpatient clinical experience, advanced clinical expertise and an extensive knowledge of complex disease processes with broad clinical experience in an inpatient setting. **Licenses, Registrations, or Certifications Required:** RN current license or RHIA/RHIT/CCS (medical school graduates are exempt from this MQ) **And** Must acquire CCDS or CDIP certification within 3 years of hire **Job Summary:** **Scope:** Responsible for the overall improvement of the quality and accuracy of medical record documentation through interaction with physicians, members of the patient care team and hospital coding staff. **Function:** Ensures clinical documentation accurately reflects the appropriate level of service provided, severity of illness, and risk of mortality of each patient. Successfully facilitates the accurate representation of patient status that translates into coded data. **Job Duties:** + Concurrently review inpatient admissions to identify opportunities to clarify missing or incomplete documentation. + Collaborate with providers, case managers, coders, and other healthcare team members to facilitate comprehensive health record documentation that reflects clinical treatment, decisions, diagnoses, and interventions. + Understand the general flow of health information from medical record documentation and discharge, through coding, to billing and finally to data reporting. + Utilize the hospital's designated clinical documentation system to conduct reviews of the health record and identify opportunities for clarification. + Apply knowledge of inpatient ICD-10 coding guidelines and clinical documentation requirements to assign working MS-DRG. + Enter review information and working MS-DRG/APR-DRG's with associated length of stay in the shared information system, and updates this information as needed to reflect any changes in patient's status, procedures and treatments. + Communicate with providers either through discussion or in writing (e.g., formal queries) regarding missing, unclear, or conflicting health record documentation for clarification. + Conduct follow-up of posted queries to ensure queries have been answered and physician responses have been appropriately documented. + Educate and communicate clinical documentation opportunities in the appropriate hospital venues for staff and physician learning opportunity. + Act as a consultant to coding professionals when additional information or documentation is needed to assign coded data. + Collaborate with HIM/coding professionals to review individual problematic cases and ensure accuracy of final coded data in conjunction with CDI managers, coding managers, and/or physician advisors. + Assume responsibility for professional development by participating in workshops, conferences and/ or in-services. + Keep current with changes in coding guidelines, compliance, reimbursement, and other relevant regulatory updates. + Contribute to a positive working environment and perform other duties as assigned or directed to enhance the overall efforts of the organization. + Maintain positive and open communication with physicians, members of the patient care team, case management and hospital coding staff. + Adhere to internal controls and reporting structure. + Comply with all relevant policies, procedures, guidelines and other regulatory, compliance and accreditation standards. + Performs related duties as required **Knowledge/Skills/Abilities:** Demonstrate excellent observation skills, analytical thinking and problem solving plus good verbal and written communication. **Preferred Qualifications:** + Bachelor of Science in Nursing (BSN) + CCDS or CDIP Certification + One year CDI experience **Salary Range:** Actual salary commensurate with experience. **Work Schedule:** Remote work, Monday through Friday, 8am to 5pm and as needed on occasion. **Equal Employment Opportunity** UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a VEVRAA Federal Contractor, UTMB Health takes affirmative action to hire and advance women, minorities, protected veterans and individuals with disabilities. Compensation $64k-93k yearly est.46d agoStatistician 3
A Statistician 3 plans, designs, and conducts advanced statistical studies & collections on various Elementary & Secondary educational programs. Veterans: * Pennsylvania law (51 Pa. C.S. A Statistician 3 works with program staff internal and external to the agency to make sure requirements are clearly understood and data is accurate and complete. If you are unable to telework, you will have the option to report to the headquarters office in Harrisburg, Pennsylvania. * One year as a Statistician 2; or $72k-103k yearly est.6d agoStatistician
Treliant's Regulatory Compliance and Risk Management practice is hiring a Statistician with a strong background in Fair Lending and related quantitative disciplines to join the team as an FTE. $69k-100k yearly est.14d agoStatistician Associate
Our Initiatives include: * Workplace Safety * Roadway Security * Impairment We are currently looking for a Statistician Associate to join us in our mission to save lives and prevent injuries. The National Safety Council is America's leading nonprofit safety advocate. $65k yearly19d agoSENIOR STATISTICIAN - Structural Heart & Aortic (remote)
In this exciting role as a Senior Statistician, you will have responsibility for statistical aspects of study design and analysis of data from complex clinical studies conducted for regulatory approval or marketing purposes. $110k-165k yearly25d agoSenior Biostatistician
This individual will work onsite in San Diego, CA, Rochester, NY, or Raritan, NJ. As we continue to grow as QuidelOrtho, we are seeking a Sr. Biostatistician to works with Biostatistics team members to provide statistical support under minimal supervision of the Biostatistics leadership. QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. The Senior Biostatistician performs data analyses and prepares presentations and publications. $107.1k-197k yearly6d agoStatistician Analyst
The Statistician Analyst will support the US Department of State in decision-making by collecting, analyzing, and presenting data. Learn more about what working at Chenega MIOS can mean for you. At Chenega MIOS, our professional development plan focuses on helping our team members at every level of their careers to identify and use their strengths to do their best work every day. If so, Chenega Military, Intelligence & Operations Support (MIOS) could be the place for you! The Statistician Analyst may work in a variety of files and use their mathematical skills to understand data trends before presenting reports to business managers and stakeholders. $71k-102k yearly est.21d agoSenior Biostatistician - Remote
Job DescriptionContact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com Job Description: As a Lead Statistician, you will be responsible for strategic statistical and 'hands on' day to day support for several studies in support of clinical programs. Serve as the lead statistician for more than one study, contribute and collaborate on study/project teams, develop the statistical design/strategy and statistical analysis plans, conduct exploratory analyses using R/SAS, design the tables, listings and figures for statistical reporting, work closely with the programming team to define ADaM specifications and review ADaM datasets, and support responses to regulatory questions. This role will contribute to Protocols, data reporting (TFLS) for CSR/DSUR/IB reporting, regulatory activities and safety assessment. This role will be a core member of the Study and Clinical Project teams, key partner with R&D colleagues and collaborate across Biometrics and RWE functions to progress the company's portfolio of clinical stage gene therapies. Responsibilities * Lead the statistical strategy for more than one study and participate as a core member on study/clinical project teams. * Be accountable and responsible for the statistical design, analysis, reporting (including development of ADaM specifications/datasets) and interpretation of Phase 1-4 clinical trials including integrated analyses across trials * Initiate, drive and implement novel methods and innovative trial designs. * Provide statistical input into protocol and case report form (CRF) development (e.g., trial design, sample size estimation, statistical methods for protocols, edit checks for clinical trial data) * Participate in regulatory (e.g., pre-IND, NDA) activities including authoring of statistical sections and participating in regulatory meetings/written responses. * Contribute to planning and execution of exploratory analyses, data visualization and statistical consultation on cross-functional teams. * Collaborate cross-functionally (e.g. data management, programming, safety, clinical, etc) to ensure timeliness and quality for statistical deliverables. * Contribute to external engagement with consultants, advisory boards, health authorities, congresses, and scientific meetings. * Write statistical analysis plans. Design and develop tables, listings and figures (mock TLFs). Partner with programming on analysis datasets and review of TLFs. * Quality assure and validate statistical outputs (TFLs) and develop/review ADaM specifications and datasets, interpret and clearly communicate statistical results and concepts to non-statisticians. * Provide statistical support and outputs for conference presentations, manuscripts, CSRs, DMCs, etc. * Develop/Write statistical standard operating procedures (SOPs) and input into general standardization efforts (e.g., CDISC, TFLs, eCRFs). * Keep abreast of new developments in statistics, drug development, and regulatory guidance through literature review and attendance at workshops and professional meetings. Qualifications * PhD in Biostatistics or Statistics with ≥ 6 years of pharmaceutical or CRO industry experience (MS candidates with significant related experience may be considered) * Experience reporting Phase 1-3 clinical trials data in CSRs to CDISC standards. * Experience supporting regulatory efforts. * Deep and broad statistical expertise in methodologies such as Mixed Models, Bayesian approaches, Interim Analyses including Futility, Modelling and Simulation methods, and in SAS, R. * Ability to work successfully within cross-functional teams leading to successful global regulatory filings and approvals. * Excellent verbal and written communications skills, strong presentation skills, able to translate statistical concepts to non statisticians. * Ability to be flexible and adapt quickly to the changing needs of the organization. * Ability to organize multiple work assignments and establish priorities. * Experience with rare diseases and/or gene therapy development preferred * Extensive SAS and R programming required. * Extensive experience reporting clinical studies to CDISC standards * Expertise and experience in ADaM specifications and datasets * Experience writing statistical analysis plans and mock TFLs for clinical study reporting. * Experience working on clinical study teams and project teams to design studies including sample size calculations. * Experience supporting DSURs, IBs and DMCs. $77k-108k yearly est.Easy Apply16d ago
Learn More About Biometrician Jobs
Average Salary For a Biometrician
Based on recent jobs postings on Zippia, the average salary in the U.S. for a Biometrician is $76,198 per year or $37 per hour. The highest paying Biometrician jobs have a salary over $132,000 per year while the lowest paying Biometrician jobs pay $43,000 per year
Updated May 25, 2023
Average Biometrician Salary
$92,601 yearly
$37 hourly