Biostatistician or Sr. Biostatistician (Home-based opportunity)

Overview:

NOTE: This role can be based remotely from any location in the U.S.

Advanced Clinical is currently seeking a Biostatistician/Sr. Biostatistician, who will be responsible for independently planning and managing project deliverables and study-level analysis and reporting activities and for providing statistical support for clinical trials.

Responsibilities:

Statistical Responsibilities:

  • Apply knowledge of statistics, statistical programming, and pharmaceutical regulations to drug development projects
  • Participate in the design and review of clinical protocols, including preparation of statistical sections, sample size calculations, randomization, and study design
  • Prepare and review statistical analysis plans (including shell tables, listings, and figures)
  • Prepare and review programming specifications used in creating derived datasets, tables, listings, and figures
  • Perform efficacy and safety analyses for clinical trials data and participate in validation and quality checks for statistical output
  • Implement and support CDISC, ICH, and other regulatory standards
  • Review CRFs, database specifications and database validation checks

Project Management Responsibilities:

  • Plan and manage project and study-level analysis and reporting activities
  • Communicate with clients and colleagues on statistical issues and project status

Standard Operating Procedures (SOPs):

  • Be familiar with and follow departments SOPs
  • Assist in creating, revising and review of departments SOPs

Business Development:

  • Assist in preparing monthly revenue reports for biostatistics
  • Assist with RFP/RFI completing and attend sales meetings as requested

Qualifications:

  • PhD or Master's degree in Statistics or a closely related field
  • A minimum of 3 years of experience as a statistician in pharmaceutical development and SAS programming for statistical analysis.
  • Candidate must have experience in clinical trial design and must be familiar with regulatory requirements.
  • Excellent oral and written communication skills, organizational skills, and attention to detail are required.
  • CDISC experience preferred

What We Offer:

  • Outstanding compensation package
  • Cutting edge tools & software
  • On-going training & development
  • Work-Life Balance – Ability to work from home
  • Strong national client base & name recognition
  • Excellent Benefits – Medical / Dental / Vision / 401K / Vacation

Advanced Group is proud to be an Equal Opportunity Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, ancestry, marital or veteran status.

For a complete list of all of our job openings, please click here


Meet Some of Advanced Clinical's Employees

Shaniya K.

Medical Writer

As a medical writer, Shaniya is responsible for compiling the data from clinical study reports, analyzing what’s been learned from conducting the trial, and summarizing that information into a scientific document.

Domantas G.

Associate Director, Clinical Monitoring

As Associate Director of Clinical Monitoring, Domantas is responsible for leading the Monitoring Team’s efforts to ensure the highest quality across clinical trials conducted at Advanced Clinical.


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