White Paper

Staffing a Phase III Program Without Losing Timeline

What sponsors get wrong when they scale clinical teams late in development, and the resourcing order that protects the critical path.

14 pagesClinical operations leaders, program managers, and study directors

Overview

A Phase III program rarely slips because one role went unfilled. It slips because the roles were filled in the wrong order. Data management arrives after database lock is already at risk. Medical writing gets engaged once the submission clock has started running.

This one maps the resourcing sequence against clinical milestones: which functions have to be in place before study startup, and which can be layered in later without much disruption. It draws on engagements where sponsors went from a handful of contributors to teams of twenty or more.

Most of the damage is done in the first six weeks.

What you will learn

  • Sequence clinical hires against startup, enrollment, and lock milestones
  • Work out where a contractor beats a permanent hire, and where they do not
  • Set onboarding expectations that get consultants productive inside two weeks
  • Plan the handoff back to internal staff after lock
Written forClinical operations leaders, program managers, and study directors
Topics
  • Life Sciences Staffing
  • Clinical Operations

How Viltis helps

Related services

The practices in this paper map to work our consultants deliver directly. If you would rather have it done than read about it, start here.

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