Associate Director, Biostatistics and Programming

Location
Remote
Salary
0
Posted
06 Apr 2021
Closes
06 May 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Senior Management

1. JOB SUMMARY/PURPOSE:   

Provides statistical leadership, direction and consulting for the design, analysis, and reporting of clinical trials.  Actively leads in the design, analysis and reporting of clinical studies.  Ensures Biometrics work is done with quality and is within timelines and budget. 

2. MAJOR RESPONSIBILITIES:  

  • Develops, guides in preparations of analysis plans, reporting specifications, and performs statistical analysis and interprets results 
  • Writes and reviews statistical sections for clinical study protocols 
  • Coordinates production of statistical and clinical reports including summary statistics, tables, listings and/or figures 
  • Reviews work of other biostatisticians 
  • Develops, modifies, and/or implements statistical techniques and processes for the analysis of clinical study data 
  • Develops innovative statistical strategies in complex new areas 
  • Provides significant input into the design, preparation and review of clinical study protocols and consults in the development of case report forms (CRFs)  
  • Prepares randomization schedules 
  • Provides leadership in statistical issues to the project team 
  • Interacts with project teams and clients including preparation of bid proposals, statistical consulting, and visits to clients to discuss statistical issues 
  • Manages department all levels of biostatistics and programming staff 
  • QC the team’s work; may occasionally need to lead studies 
  • Works with functional and project managers to determine resources projections and project schedules 
  • Leads BM hiring process and creates study assignments for BM staff 
  • Provide support to Biostatistics and Programming department consulting efforts including design and protocol development for potential sponsors. 

3. QUALIFICATIONS:   

  • MS or PhD (preferred) in Statistics or Biostatistics  
  • Progressive experience working with SAS or a comparable statistical package 
  •  Experience as a manager or team lead with statisticians and/or SAS programmers 
  • Experience with the statistical aspects of a Phase I-III clinical trial 
  • Proficient oral communication and presentation skills 

4. LEADERSHIP COMPETENCIES:   

  • Demonstrates ethics and integrity 
  • Displays drive and purpose 
  • Exhibits leadership stature 
  • Holds self and others accountable for measurable high-quality, timely, and cost-effective results 
  • Adapts to an ever-changing environment 
  • Develops new insights into situations and questions conventional approaches 
  • Develops networks and builds alliances; collaborates across boundaries to build strategic relationships and achieve common goals 
  • Perceives organizational and political reality and acts accordingly 
  • Formulates objectives and priorities, and implements plans consistent with the long-term interest of the organization 
  • Takes a long-term view and builds a shared vision with others 

Apply for Associate Director, Biostatistics and Programming

Already uploaded your CV? Sign in to apply instantly

Apply

Upload from your computer

Or import from cloud storage

Your CV must be a .doc, .pdf, .docx, .rtf, and no bigger than 1MB


4000 characters left

Marketing Communication

We'd love to send you information about Jobs and Services from PharmiWeb.jobs by email.

All emails will contain a link in the footer to enable you to unsubscribe at any time.


When you apply for a job we will send your application to the named recruiter, who may contact you. By applying for a job listed on PharmiWeb.jobs you agree to our terms and conditions and privacy policy. You should never be required to provide bank account details. If you are, please email us.

Similar jobs

Similar jobs