[ref. u06041617] View Jobs Description - Baltimore

apartmentLMR Technical Group placeBaltimore calendar_month 

LMR Technical Group (LMR) is seeking a Biostatistician Data Manager.

Location: Baltimore, MD. Teleworking eligible.

Job Description: The Biostatistician Data Manager will independently provide expert biostatistical support to the Brain Health Equity (BHE) Unit within the Health Disparities Research Section (HDRS) at the National Institute on Aging (NIA). The primary objective is to assist in the statistical design, analysis, and interpretation of data from community-based cohort studies and other research projects led by the Principal Investigator.

Duties and Responsibilities:

  • Assists in performing a variety of data management and analytical tasks and organizing complex, large-scale datasets.
  • Provide biostatistical expertise for the research study.
  • Analyze, interpret, communicate and document epidemiologic data and results.
  • Provide analytic results using standard statistical procedures, including descriptive statistics, rate standardization, stratification of data
and model building (logistic regression, conditional logistic regression, Cox regression) using SAS, Stata, Epicure, and similar statistical
software programs.
  • Collaborate and work with a team of researchers to develop, iterate and execute innovative strategies for genomic data integration and
modeling/prediction.
  • Utilizes statistical software packages to manage, maintain and analyze large, complex statistical datasets.
  • Work with branch staff and research training fellows to provide statistical support for studies based on existing data sets; work with
staff to assemble data sets for these purposes.
  • Enter and verify data fields and data dictionaries.
  • Perform descriptive and missing data analysis.
  • Documents analyses performed and prepares progress reports summarizing results.
  • Prepare summaries and reports for staff review.
  • Write statistical sections in manuscripts; work with research staff to interpret referees’ comments on manuscripts.
  • Provide description of statistical methods in manuscripts; work with research staff to respond to and interpret referees’ comments.
  • Performs a variety of data management and analytical tasks and organizing complex, large-scale datasets.
  • Provide biostatistical expertise for the research study.
  • Analyze, interpret, communicate and document epidemiologic data and results.
  • Communicate research findings, disseminate public information and respond to relevant inquiries.
  • Provide analytic results using standard statistical procedures, including descriptive statistics, rate standardization, stratification of data
and model building (logistic regression, conditional logistic regression, Cox regression) using SAS, Stata, Epicure, and similar statistical
software programs.
  • Collaborate and work with a team of researchers to develop, iterate and execute innovative strategies for genomic data integration and
modeling/prediction.
  • Conducts statistical analyses on completed and ongoing studies utilizing a wide range of standard and non-standard statistical
software packages for all projects.
  • Write code to execute data analysis, visualize and provide interpretation and context to results of analysis.
  • Perform descriptive and missing data analysis.
  • Perform data cleaning (identifying and correcting data entry errors and/or missing values) and data transformation (creating and
categorizing variables and imputing data).
  • Reviews and summarizes relevant literature and other sources to develop analytical plans.
  • Consult with staff on the application of statistical methods to address the key study scientific aims of the study.
  • Provide literature review related to analyses used in comparable studies.
  • Learns and applies new statistical methods and software packages and provides consultation and training to other analysts and
staff.
  • Integrate data from multiple sources into SAS data sets.
  • Develop and implement new research and study designs using appropriate statistical methods.
  • Research and analyze new developments in biostatistical methods and applications.
  • Deliverables
  • Study Design and Protocol Documentation: Work products related to the design of research studies, development of statistical analysis
plans, and study protocols. - Ad-Hoc
  • Data Analysis Reports: Statistical reports, tables, and figures derived from analyses of study data. These should include documentation of the statistical methods used and the results obtained. - Ad-Hoc
  • Data Management Documentation: A comprehensive codebook, data dictionaries, and documentation of data management practices, including data cleaning and coding processes. - Ad-Hoc
  • Compliance and Quality Assurance Reports: Documentation ensuring compliance with Institutional Review Board (IRB) requirements and quality control processes for data integrity and security. - Ad-Hoc
  • Data Sharing Oversight: Ensure that data is shared only with investigators who have approved project proposals and are employed by institutions with active data-sharing agreements. Provide documentation verifying that data distribution adheres to these protocols. - Ad-Hoc
  • Project Proposal Review: Provide assessments to the Principal Investigator regarding the originality of proposed research, recommending alterations in project proposals to avoid duplication of work or efforts within ongoing studies. - Ad-Hoc
  • Presentation and Publication Materials: Prepare manuscripts, abstracts, and presentations, summarizing statistical findings for publication or presentation at scientific conferences. - Ad-Hoc
  • Training Materials: Develop materials for training junior staff or collaborators on statistical methods, data analysis software, and
proper data management protocols. - Ad-Hoc
  • Data Sharing Integrity Reports: Document all data-sharing activities, ensuring the security and integrity of distributed data. Use independent judgment to advise on data sharing decisions and maintain records of data requests and transfers. - Ad-Hoc
  • Other related duties as assigned

Basic Qualifications:

  • Master’s or Ph D in Biostatistics, Statistics, Bioinformatics, or a related field with specialized experience in statistical analysis of
epidemiological data. A bachelor's degree with extensive specialized experience may be considered.
  • Minimum of five years of related experience.
  • Proficiency in statistical software such as R, Mplus, SPSS, and other statistical computing software.
  • Strong analytical and problem-solving skills, with the ability to independently design and implement statistical analyses for complex
datasets.
  • Extensive experience in the application of statistical methods to public health, epidemiology, or clinical research, particularly within the
context of community-based cohort studies.
  • Excellent communication skills, with the ability to clearly explain statistical concepts and results to non-statistical audiences.
  • Experience in data management, including data cleaning, coding, and ensuring data integrity.
  • Knowledge of regulatory requirements and guidelines related to data protection and research ethics.
  • Knowledge of regulatory requirements and guidelines related to data protection and research ethics.
  • Ability to work independently and as part of a multidisciplinary team.
  • Must have the correctible near vision and the ability to distinguish basic colors.
  • Must be legally authorized to work in the United States without the need for employer sponsorship, now or at any time in the future.

Preferred Qualifications:

  • Prior experience working with the National Institute of Health (NIH).
  • This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required by this position.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

LMR's Benefits Plan Includes:

  • Medical, Dental, and Vision Insurance
  • Life and Disability Insurance
  • 401(k)
  • Paid Time Off
  • Paid Holidays
  • Employee Assistance Program
About LMR:

LMR is a service-disabled veteran-owned small business that supports technology development and provides comprehensive joint warfighter training by leveraging the skills, experience, and knowledge of its personnel. Our team consists of personnel with diverse backgrounds.

LMR is an equal opportunity organization. We recruit, employ, train, compensate, and promote without regard to race, religion, color, national origin, age, gender, sexual orientation, gender identity, marital status, disability, protected veteran status, or any other basis protected by applicable federal, state or local law.

LMR will not discriminate against persons because of their disability, including disabled veterans, and will make reasonable accommodations for known physical or mental limitations of qualified employees and applicants with disabilities. If you are interested in applying and require special assistance or accommodations due to a disability, please contact our Human Resources department at hr@lmrtec.com.

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