Senior/Principal Biostatistcian Consultant remote (Infectious Disease

ClinChoice

$120K — $140K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • MS or PhD in Statistics, Biostatistics, or related field
  • Deep expertise in statistical methods like Poisson regression and time-to-event analysis
  • Proficiency in experimental design and both descriptive and inferential statistics
  • Experience in pharmaceutical or related industries, particularly with clinical trials
  • Strong oral and written communication abilities
  • Proficient in programming languages such as SAS or R.

Responsibilities

  • Serve as the study statistician for Bronchiectasis or Hepatitis B programs
  • Develop protocols including study design and statistical analysis plans
  • Oversee statistical quality and consistency across studies
  • Ensure accuracy and completeness of data for statistical analyses
  • Prepare and verify the timely delivery of statistical input for reports
  • Identify and rectify flaws in statistical reasoning and interpretation
  • Maintain consistency of statistical visuals and report text.

Benefits

  • Remote work opportunity
  • Exposure to innovative therapeutic areas like infectious diseases and vaccines
  • Collaboration with a cross-functional team in a dynamic environment
  • Professional development and continued education opportunities
  • Opportunity to impact clinical trials in critical therapeutic areas.
Full Job Description
Main Job Tasks and Responsibilities:

  • Serve as study statistician or support statistician on Bronchiectasis or Hepatitis B programs

Primary Responsibilities:
  • Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.
  • Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.
  • Responsible for assuring that data for statistical analyses are complete, accurate and consistent.
  • Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.
  • Responsible for validity of analysis and alternative analysis strategies when unforeseen circumstances arise.
  • Demonstrates extensive understanding of statistical concepts and methodologies. Recognizes and corrects flaws in scientific reasoning and statistical interpretation.
  • Responsible for accuracy and consistency of statistical tables, figures, and data listings, accuracy of report text, and consistency between summary tables in the body of reports and the corresponding source tables and listings.
  • Responsible for statistical methods section for the reports. Identifies and corrects common flaws in interpretation of results, inconsistency in presentation or inference, adherence to the report guidelines, and assures project-wide consistency.

Qualification:
  • MS or PhD in Statistics, Biostatistics or related field.
  • High degree of technical competence
    • Understanding of Poisson regression or negative binomial methods, time to event, or multiple imputation methods
  • Competent in experimental design, descriptive and inferential statistics.
  • Pharmaceutical or related industry experience with clinical trials.
    • Vaccines or infectious disease experience preferred but not essential
  • Excellent communication skills, both oral and written.
  • Excellent programming skills (SAS/R)


The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

#LI-TT1 #LI-Remote #LI-Principal #Contract

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