Randstad USA Disability

Job Information

Randstad Director, Clinical Project Management in Waltham, Massachusetts

Director, Clinical Project Management

job details:

  • location:Waltham, MA

  • salary:$90 - $100 per hour

  • date posted:Wednesday, March 20, 2019

  • experience:5 Years

  • job type:Contract

  • industry:Professional, Scientific, and Technical Services

  • reference:28178

job description

Director, Clinical Project Management

job summary:

The Director of Project Management provides project leadership to cross-functional teams in the successful delivery of all phase drug development projects or sub projects within a major development program. These responsibilities include leadership of the team in predicting and planning solutions to achieve successful operational execution; driving the team to achieve clarity on issues and focus on effective contingencies; interfacing with senior management and influencing decision-making on projects. This position will have a high level of interaction with Senior Management to ensure that the scientific strategy is clearly integrated into operational plans.?

location: Waltham, Massachusetts

job type: Contract

salary: $90 - 100 per hour

work hours: 9 to 5

education: Masters


  • Leads the planning efforts for assigned development programs in defining and implementation of Project Team strategy and operational plans.

  • Manages the operational plan and formulates the project scope, project plan, critical paths and risk-mitigation strategies with the Project Team and the Senior Management team.

  • Identifies and drives project and resource priorities that align with the business objectives that identify ways to accelerate the project execution where possible while maintaining high quality standards.

  • Develops strong logistical skills to manage activities across functions and regions.

  • Manages the identification and escalation of potential issues/risks or obstacles and achieves resolution or plans contingencies and follow issues through to resolution ensuring that all issues arrive at a singular conclusion or recommendation.

  • Establishes, communicates and executes plans that drive toward goal achievement.

  • Generates collaboration, cooperation and communication across functions teams to achieve stated goals.

  • Responsible for setting and managing expectations, highlighting and resolving issues, ensuring regular communications and managing internal and external activities. Facilitates the system to track and monitor program objectives/goals.

  • The scope of responsibilities extends from early clinical development through commercialization and post-marketing commitments.


  • Requires a Master's degree and a minimum of 5-7 years' experience as a project manager leading complex pharmaceutical projects in a multi-disciplinary, global environment. PhD, MD or PharmD a plus.

  • Extensive drug development experience with biologics in Phase 1-IV and Commercialization is preferred.

  • Proven leadership experience in managing a global, cross-functional team with demonstrated skills in strategic planning, risk mitigation, and operation problem solving.

  • Solid working knowledge of functional IND, BLA and NDA components/requirements required. Ideal candidate has worked on a program(s) that lead to successful regulatory approval (i.e., NDA, BLA, MAA, or SNDA).

  • Excellent verbal, written, and organizational communication skills.

  • Proficient in Microsoft Office including Word, Excel, PowerPoint, Microsoft Project and Outlook

skills: Phase iii

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.