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Director of Project Management- CRO

Reference

DD2502DC

Location

Boston, Massachusetts

Salary Range

$115,000 - $130,000

job description

Chase Weston has partnered with a global Contract Research Organisation who are looking for an individual with excellent project management experience to act as the lead on multiple client projects at any one time. The role can be based in either of the companies key offices; New Jersey or Massachusetts.

Key Responsibilities:

  • Ensure effective balance of time, cost, quality and risk so that regulatory and project management/execution strategies meet the needs of the client
  • Work cross-functionally to ensure the relevant project team has appropriate resourcing to meet objectives
  • Take initiative to identify opportunities for continual improvement, and propose, develop, and implement such opportunities
  • Support the project life cycle, including project planning, tracking, controlling, budgeting, reporting, proactive issue/risk management, and effective project finish

Qualifications/Requirements:

  • Bachelor’s Degree required (life sciences disciplines strongly preferred)
  • 6+ years’ relevant experience in project management or regulatory affairs or related functions in drug/biologics development/manufacturing
  • Excellent industry knowledge and familiarity with the drug development process, US regulations, and ICH, FDA, and EMA guidance, and the organization of the common technical document (CTD).  Includes in-depth knowledge of GxP, ICH, FDA, EMEA and other relevant guidelines
  • Create and explain Gantt and RACI charts and other representations of project and program timelines
  • Previous people management experience within a matrix environment
  • Ability to travel 10-15%, including inter-office travel
  • IT skills, including Microsoft Office Suite (Word, Project, PowerPoint and Excel) and Adobe Acrobat

Job Reference: DD2502DC

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