Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community.

KEY RESPONSIBILITIES:

• Develops and analyzes a variety of research data using statistical methods.
• Assists researchers in developing appropriate study protocols and computer analyses.
• Manages computer systems, writes programs, and trains others in the use of systems.
• Keeps abreast of the latest statistical modeling and computing tools.
• Participates in the development and selection of appropriate statistical methods and tests, sample size calculations and creation of randomization schedules.
• Prepares statistical method sections for inclusion in study protocols.
• Reviews the design and content of database designs and data edit checks.
• Develops and validates SAS programs to support statistical analyses.
• Provides interpretations of statistical results, and prepares the relevant statistical sections for study reports.
• Creates and maintains biostatistical documentation, including descriptions of methods, SAS programs and results.
• Prepares electronic files using appropriate formats for submission to regulatory agencies.
• Participates in the development of standardization procedures for statistical functions.
• Reviews and audits statistical analysis plans, SAS programs, and statistical reports including tables, listings, and figures.
• Provides guidance to more junior biostatisticians.
• Evaluates and proposes new statistical methods for data analysis.
• Assigns and monitors activities of other project personnel.
• Assist in setting priorities of work to be done.
• Provides support and serves as a resource to biostatisticians, programmers, and data analysts.
• Participates in training of less senior biostatisticians and other team members.
• Provides input into the evaluation of their team members.
• Reviews and helps prepare statistical and database management sections of NIH grant applications and other externally supported proposals prior to submission.
• Writes statistical methods section of manuscripts for publication.
• Writes and/or revises quantitative, epidemiologic, and medical sections of manuscripts.
• Helps estimate budgets for biostatistical support for larger, more involved clinical studies (NIH program project grants, multicenter clinical trials etc).
• Monitors data collection, institutes procedures to assure data quality and guarantees study protocols are followed appropriately.
• Performs related responsibilities as assigned.

ADDITIONAL JOB DETAILS:

• Works with faculty or staff biostatisticians to provide study design expertise (scientific collaboration) to investigators/researchers interested in conducting a variety of clinical studies (both retrospective and prospective studies).
• Consults with investigators to determine an important question of interest that will yield new knowledge and identify the outcome appropriate to address that question.
• Learns to develop and implement data management and quality control plans for larger clinical studies within a team-science environment; Learns fundamentals of using data management software (query system and edit checks for quality control).
• The selected candidate will perform routine statistical analyses under the supervision of faculty and/or staff (senior/lead/principal biostatisticians) in a team science environment.
• This work can be done through short-term consulting projects or through a team science model for larger long-term clinical studies.
• Expectations include basic knowledge of study design, continual expansion of statistical programming skills, strong organizational and time management abilities, and excellent oral and written communication skills on scientific and technical issues.
  
• Works with faculty or staff to draft statistical methods, the data management plan, and Results section for medical manuscripts; Documents methods and results through preparation of memoranda and reports.
• The biostatistician regularly attends meetings with more experienced statisticians to develop the skills necessary to be an effective consultant.
• The primary goal of the biostatistician is to work with the medical investigator to develop a clear, mutual understanding of the clinical research problem.
• Success requires clear, broad, specific two-way iterative communication on both scientific issues and research roles (not technical issues).
• This type of interaction should lead to better designed studies in the future.
  
• Continues to develop statistical programming skills (SAS, R, STATA).
  
• Refines technical writing skills necessary to summarize the results of analysis based on implementation of a statistical analysis plan.
  
• Invests time to learn both a generalist’s breath and a specialist knowledge to effectively collaborate on medical research projects; The statistician must learn to effectively communicate with medical investigators on scientific issues.

MINIMUM QUALIFICATIONS:

• A bachelor's degree in statistics, biostatistics, computer science, or a related field and two years related experience, OR an equivalent combination of education, training, and/or experience.

PREFERRED QUALIFICATIONS:

• A master's degree in statistics, biostatistics, epidemiology, or a related field.
• We are seeking a candidate (minimum of 2 years of experience OR an equivalent combination of education, training, and/or experience) with a background in statistics, biostatistics, epidemiology, and/or other related quantitative field, to join our group of clinical biostatisticians in the Emory School of Medicine.
• Consults with investigators to determine an important question of interest that will yield new knowledge and identify the outcome appropriate to address that question.
• Attention to schedule (deadlines) and accurate assessment of time needed to complete projects.
• Ensures good clinical practice through quality data (data and reported results are credible and accurate) and ethics (security and confidentiality of subjects’ data are protected).
• Develops expertise in the design and development of Case Report Forms (CRFs) based on the data collection requirements dictated by the study protocol and manual of procedures.
• Designs and generates tables and statistical graphics needed for medical manuscripts; Works with faculty or staff to address issues identified through peer review of medical manuscripts.
• Leans to identify and draft a description of study limitations that should be communicated to the reader of peer reviewed studies.
• This level of work may result in co-authorship where two statisticians from the clinical science team earn co-authorship on a clinical paper.

NOTE: This role will be granted the opportunity to work from home regularly but must be able to commute to Emory University on a flexible weekly schedule based upon business needs.  Schedule is based on agreed upon guidelines of department. This role requires residency in the state of GA. Emory reserves the right to change remote work status with notice to employee.

Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: 404-727-9867 (V) | 404-712-2049 (TDD).

Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination.