Biostatistician with R

IT Engagements

  • NULL, NULL
  • 13 days ago
  • Remote
  • $65–$70

Highlights

Job Title: Biostatistician with R (Contract Role) Location: 100% Remote Years of experience: 4+ Years Duties: Performs analyses of clinical and digital biomarker data and prepares tables/figures to show and explain the results. Greetings from IT Engagements IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions.

Numbers & Facts

LocationNULL, NULL (
Remote
)
Salary$65–$70

Description

Greetings from IT Engagements
IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients.
Job Title: Biostatistician with R (Contract Role)
Location: 100% Remote
Years of experience: 4+ Years
Duties:
  • Performs analyses of clinical and digital biomarker data and prepares tables/figures to show and explain the results
  • Prepares statistical analysis plans in both slide and text form
  • Prepares summaries of exploratory analyses, in both slide and text form, and presents results to both statisticians and non-statistician collaborators
  • Performs quality control and pre-processing of data collected with digital health technologies
  • Creates and optimizes statistical computing scripts (R and/or Python)
  • Collaborate on developing case report forms and clinical database to ensure quality data collection
  • Lead the efforts of data analysis for data monitoring committee as needed
  • Develop and maintain statistics programming
  • Deliver statistical expertise and knowledge to internal and external stakeholders
  • Create statistical programs that can analyze, and report information from large databases
Qualifications:
  • Master's degree in Biostatistics, Statistics or related field with 4 years of previous analytical experience in clinical trials
  • Must be proficient with SAS and/or R
  • Knowledge in statistical methodologies related to clinical trial designs, statistical modeling and data analyses
  • Knowledge and understanding of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical or Medical Device research setting.
Thank You
Satya
Satya@itengagements.com

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