Project Manager, Central Laboratory Services

3 hours, 56 minutes ago
Full-time
Senior
Project and Program Management
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012

Description

  • Lead and manage assigned central laboratory projects from conception through close-out.
  • Serve as the cross-functional lead and main client-facing partner for new and ongoing studies.
  • Create, maintain, and report on project timelines, budgets, revenue goals, forecasts, and resource plans.
  • Coordinate daily project activities, delegate responsibilities, and supervise scheduled work.
  • Communicate with clients, collaborators, vendors, and internal teams on data management, inventory control, shipping, and related topics.
  • Prepare and present project updates, reports, and correspondence for internal and external meetings.
  • Monitor project scope, identify out-of-scope work, and escalate issues with action plans.
  • Assess, mitigate, and resolve technical, operational, project, and business risks and issues.
  • Review, update, and maintain project documentation and process documents to approvable status.
  • Mentor junior Project Managers and support senior staff as needed.

Requirements

  • Bachelor's degree in a life science or related field such as engineering.
  • Experience as a Project Manager in Central Laboratories for a CRO, pharmaceutical, or biotech company.
  • Excellent listening and communication skills.
  • Excellent computer skills with MS Office/MS 365 applications.
  • Strong understanding of project management and data analysis.
  • Strong critical thinking, analytical, and problem-solving skills.
  • Excellent presentation, interpersonal, organizational, and multi-tasking skills with exceptional emotional intelligence.
  • Exceptional research, reporting, judgment, and discretion skills.
  • Fluency in reading, writing, speaking, and understanding English.
  • Ability to travel domestically and internationally, including overnight stays, approximately 10-25%, and work extended hours when needed.

Benefits

  • Remote work from Poland, Serbia, Romania, Hungary, Slovakia, Spain, or the UK.
  • Opportunity to work on global projects focused on accelerating novel therapeutics.
  • Equal Opportunity Employer status.
  • Reasonable accommodation support for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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