Senior Statistical Advisor-Canada

Indero

$100K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of relevant statistical experience in clinical trials
  • Proficiency in statistical analysis and methodologies
  • Strong communication skills for client interaction
  • Experience in protocol development and statistical analysis plans
  • Ability to interpret and present data to non-statistical stakeholders
  • Knowledge of regulatory requirements and industry guidelines
  • Experience in developing and implementing SOPs for statistical processes

Responsibilities

  • Provide statistical input on trial design and sample size estimation
  • Communicate with clients regarding statistical analysis issues
  • Review and validate statistical analysis plans and clinical trial data
  • Aid scientific writers in developing Clinical Study Reports
  • Advise on efficient design for clinical trials and research projects
  • Contribute to the development of statistical SOPs and standardization efforts
  • Collaborate with clinical trial teams and stay updated on industry developments

Benefits

  • Flexible work schedule
  • Permanent full-time position
  • Comprehensive medical, dental, and vision benefits
  • Retirement savings plan (RRSP)
  • Generous vacation and personal days
  • Access to a virtual medical clinic
  • Public transportation rebates and social activities
Full Job Description
Description

The Senior Statistical Advisor will provide statistical input into Phase I - IV clinical trial development, assist in protocol development, customer relationships, support statistical requirements for submissions, support data analysis and interpretation and support research and development. In addition, this position is required to conduct all these activities in conformance with applicable regulatory requirements, industry guidelines, and Innovaderm standard operating procedures (SOPs) while respecting Innovaderm's commitment to sponsor's requirements and timelines.

Requirements

More specifically, the Senior Statistical Advisor must:

  • Provide statistical input into protocols (e.g., trial design, sample size estimation, power calculations, randomization, statistical methods for protocols).
  • Communicate with clients regarding study protocol or statistical analysis issues.
  • Review statistical analysis plans.
  • Review clinical trial data results representing the outcome of the trial, validating statistical output, accurately interpreting, and clearly communicating statistical results and concept to non-statisticians.
  • Provide support to scientific writers working on Clinical Study Reports.
  • Advise on the design of valid, efficient, and cost-effective clinical trials and other research projects.
  • Provide input into statistical standard operating procedures (SOPs) and general standardization efforts (e.g., statistical methodology standards, standard data presentations).
  • Collaborate effectively with members of clinical trial implementation teams, and keep abreast of new developments in statistics, drug development, and regulatory guidance through literature review.

Employee may be assigned to other responsibilities that do not pertain to their former description, if they havE the required experience, are qualified and/or have received adequate training.

As a Senior Statistical Advisor, you will be eligible for the following perks:

  • Flexible work schedule
  • Permanent full-time position
  • Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities)
  • Ongoing learning and development

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