Employment

Employment Opportunities

Data Scientist (Faculty, Non-Tenure Track Research Associate)

General Summary/Purpose:

The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University fosters team science efforts, providing an environment where statisticians can advance standard statistical pipelines and cutting-edge quantitative science methodologies for state-of-art clinical studies. Thus, the members of the Division of Quantitative Sciences have strong collaborations with Cancer Center investigators and quantitative science Departments in the broader Johns Hopkins University, including the Departments of Biostatistics and Epidemiology in the Bloomberg School of Public Health.  This collaborative, transdisciplinary research and educational environment promoted by the Cancer Center and the broader Johns Hopkins University fosters a diverse and inclusive community, featuring strong mentorship and a career-path for faculty statisticians.

The Data Scientist collaborates independently with principal investigators in statistical design and analysis of clinical and laboratory studies.  Supervises and coordinates the work of staff statisticians, ensuring the appropriate and best use of standard and non-standard statistical methodologies for the design of studies and statistical analysis.  Functions largely independently or as co-investigator to solve problems posed by clinical and laboratory investigators (including meetings, experimental design, analysis, and interim and final reports), and works with the Director of Oncology Quantitative Sciences Division and the Biostatistics Shared Resource Director of the Cancer Center  to introduce and integrate novel analysis methods into the work of the statistical team as needed.

Specific Duties/Responsibilities:

  • Serve as the Lead Biostatistician in projects with standard designs
  • Participate in team science projects serving as statistician in the Biostatistics Core of SPOREs, P01s and U54s
  • Delegate duties to Biostatisticians working on the projects, providing coordination, oversight, direction and guidance as necessary
  • Monitor and coordinate the team’s effort to meet project timelines and to ensure quality standards are met
  • Consult independently with clinical and laboratory investigators to determine their needs with respect to the statistical design of studies and propose appropriate designs and analysis methods
  • Collaborate with investigators in the preparation of presentations and publications, making significant contributions to publications
  • Determine, research, and implement appropriate methodologic procedures for analysis of complexed data
  • Determine study design, perform sample size and power calculations, generate randomization schema, and write statistical sections for research protocols and manuscripts
  • Conduct statistical analysis and interpret the results. Prepare interim and final reports of studies. Discuss with colleagues, investigators, and supervisor the need for any additional analyses and/or special methodologic requirements
  • Manage computational workflows/pipelines to complete statistical or applied quantitative projects in an efficient and timely manner
  • Participate on the Protocol Review Committee

Supervision of Others:

Lead and supervise 1 – 2  junior Biostatisticians. 

Minimum Qualifications:

Education:

  • Required: Doctoral or Master’s degree in biostatistics, statistics, mathematics, data science, or related field

Experience

  • Candidate with a Master’s degree must have a minimum of 5 years of post-graduation experience
  • Recent graduates with a PhD degree are encouraged to apply

Experienced in cancer clinical trials and/or other cancer-related studies including study design and data analysis preferred

Special Knowledge, Skills, and Abilities:

  • Strong interest in collaborative research
  • Excellent leadership and project management skills
  • Basic coaching and mentoring skills
  • Solid knowledge and expertise in statistics and its applications in laboratory, and clinical and translational research, demonstrated by publications
  • Experience with implementation of novel methods and/or innovation strategies
  • Organization and management skills: Ability to work independently and as part of a team; demonstrated time management skills; ability to multitask and assign priorities; demonstrated ability to manage highly detailed projects; ability to provide continuous quality and service improvement
  • Expert knowledge of procedural-oriented statistical languages, such as SAS, and/or R.  In addition, a knowledge of other programming languages, such as Python is helpful
  • Excellent interpersonal skills in consulting with researchers and understanding their problems
  • Excellent writing and verbal skills in the preparation and presentation of reports. Attention to details is required

Please submit your Resume and three letters of reference here:

Sr. Biostatistician

General Summary/Purpose:

The Cancer Center fosters team science efforts, providing an environment where statisticians can advance standard statistical pipelines and cutting-edge quantitative science methodologies for state-of-art clinical studies. Thus, the members of the biostatistics shared resource have strong collaborations with Cancer Center investigators and quantitative science Departments in the broader Johns Hopkins University, including the Departments of Biostatistics and Epidemiology in the Bloomberg School of Public Health.  This collaborative, transdisciplinary research and educational environment promoted by the Cancer Center and the broader Johns Hopkins University fosters a diverse and inclusive community, featuring strong mentorship and a career-path for staff statisticians.

This individual is responsible for the statistical design and analysis of clinical and laboratory studies. Coordinates the use of standard and non-standard biostatistics or bioinformatics methodologies for the design of studies and the production of statistical analyses. Collaborates with investigators in the preparation of presentations and publications. Functions largely independently to solve problems posed by clinical and laboratory investigators with supervision by faculty members or Principal Biostatisticians.

Specific Duties/Responsibilities:

  • Consults with clinical and laboratory investigators to determine their needs with respect to statistical design of studies and proposes appropriate designs.
  • Recommends appropriate methodologic procedures for statistical analysis; Conducts data analysis.
  • Performs sample size and power calculations, generates randomization schema.
  • Prepares written reports of statistical analyses, including relevant statistical theory, references, methods, results, and conclusions.
  • Writes statistical design, methods, and analysis sections for research proposals and clinical trial protocols.
  • Prepares interim and final reports of studies, and progress reports.
  • Discusses with colleagues, investigators, and supervisor the need for any additional analyses and/or special methodologic requirements.
  • Participates on the Protocol Review Committee
  • Keep abreast of technical and academic resources related to statistical methodology relating to study design and analyses.

Minimum Qualifications:

Master’s degree in biostatistics, statistics, mathematics, epidemiology, or related quantitative field required.
Three (3) years of related experience required.
Demonstrated ability on significant graduate project or additional doctoral education may substitute for experience to the extent permitted by the JHU equivalency formula.

JHU Equivalency Formula: Demonstrated ability on significant graduate project or additional doctoral education may substitute for experience. For jobs where equivalency is permitted, up to two years of non- related college course work may be applied towards the total minimum education/experience required for the respective job.

Preferred Qualifications:

Five (5) years of experience is strongly preferred.
Proficiency with the statistical package SAS and/or R. Experienced in cancer clinical trials and/or other clinical research-related studies including study design and data analysis preferred.

Special Knowledge, Skills, and Abilities:

  • Expert knowledge of statistical languages, such as SAS or R.
  • Knowledge of other programming languages, such as Matlab, Python, or C++, and database management (RedCap, SQL) is helpful but not required.
  • Excellent interpersonal skills in consulting with researchers and understanding their problems.
  • Excellent writing and verbal skills in the preparation and presentation of reports.
  • Excellent organizational skills and attention to details are required.

Submit online application here:

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