Knowledge Repository

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Project Overview

Being a Statistical Programmer in the Pharmaceutical Industry is more than just knowing how to write programming code. Besides strong technical skills, such a role requires comprehensive understanding of the clinical development process, underlying regulations, industry standards and medical knowledge.

This Knowledge Repository aims to serve as a quick reference guide. This will be achieved by identifying and referring to already existing material, which will be organised in a user-friendly structure. The project will look to split into 8 different sub-groups:

  • Drug Development Process
  • Clinical Study Design and Conduct
  • Clinical Study Workflow
  • Clinical Documents
  • Regulatory Environment
  • Programming
  • Data Standards
  • Therapeutic Areas

Team meeting frequency across the sub-groups will be no more than 1 hour fortnightly, and no less than 1 hour monthly

Project members will be required to research and curate materials already published

Meeting agendas and minutes will be stored in the projects Teamwork area (access to project members only)

If you would like to join this project, please email wendy (at)

Project Leads

Beate Hientzsch Co-Lead PHUSE
Brigitte Bernhoff Co-Lead UCB
Wendy Dobson Project Manager PHUSE

Project Members

Mani Bakthavatsalam Participant Sarepta
Raghava Regulla Participant Bayer
Sandra VanPeltNguyen Participant Pfizer
Shalini Dwivedi Participant Kinapse
Zuzana Rehm Participant GSK
Murphy Wassereau Participant Industry
Faheeza Rangunwala Participant GCESolutions
Lily Chen Participant Industry
Roopali Lakhe Participant Bayer
Bhavna Nanda Participant Kinapse
Sumit Gogate Participant Industry
Andrea Palluch Participant Industry
Alexandra Cochinaire Participant JNJ

Objectives and Timelines

Initialise Project September/October 2019
Webinar Presentation - Call for Volunteers October 2019
Kick Off November 2019
Build Team & Sub-teams December 2019
Populate Education Website (at least one sub-team content) March 2020