Senior Project Manager, CMC

Project ManagerProject ManagerFull TimeRemoteSeniorTeam 1,001-5,000H1B SponsorCompany SiteLinkedIn

Location

Italy

Posted

38 days ago

Salary

0

Seniority

Senior

Postgraduate Degree8 yrs expEnglish

Job Description

Senior Project Manager, CMC

Sia

• Providing consulting services for Sia’s clients in the life sciences and healthcare industries, including but not limited to: Provide strategic oversight to maintain alignment of project milestones with day-to-day activities. • Responsibility for content, quality, and distribution of project management deliverables (reports, dashboards, etc.) and routine updates (schedule, budget, risk), typically as the final reviewer. • Establish strong working relationships with leadership and project functional teams across all levels. • Serve as project spokesperson and facilitate communications with all internal and external stakeholders (meetings, reports, etc.). • Work with cross-functional teams (CMC, Med. Affairs/Clinical, Nonclinical, Quality, Regulatory, Finance, Legal, Contracts Management, etc.) to drive project activities against scheduled timelines, approved scope, and approved budget. • Manage project financials, including vendor invoice review/approval, budget development, actuals tracking, maintenance of time-phased financial forecast, preparation of project financial reports for internal and external stakeholders. • Proactively manage strategic risks and issues, providing expertise in the identification and implementation of risk mitigation activities. • Demonstrate and foster excellent teamwork, with the ability to navigate within multidisciplinary teams. • Balance project demands to align/realign Budget, Quality, Timeline, and Scope, as needed. • Lead product development meetings, and ensure all Project Leaders, and/or subteam leaders, have all the information and support needed to implement the project. • Focus on customer service, with agility and clear communication. • Adhere to Sia quality standards regarding client deliverables.

Job Requirements

  • 8+ years of experience in the biopharmaceutical industry with a minimum of 5 years of project management experience.
  • BS, MS, or PhD in a scientific or engineering discipline (e.g., Chemistry, Biochemistry, Chemical or Biomedical Engineering, Pharmaceutical Sciences)
  • Experience working with CDMOs to support outsourced development and manufacturing activities, including oversight of deliverables and timelines.
  • Ability to engage in technical and scientific discussions.
  • Strong communication and interpersonal skills, with the ability to influence, collaborate, and build alignment across diverse technical and leadership teams.
  • Proficiency in Planisware and principles to plan, manage, and track multiple parallel projects in a complex, matrixed environment.
  • Fluent and articulate communication in English (written and spoken).
  • Excellent written and oral communication, presentation, problem-solving, and negotiation skills with an emphasis on building consensus.
  • Ability to work independently and in collaboration with others.
  • Flexibility and ability to deal with ambiguity, and a sense of personal ownership of deliverables and results.
  • Works well with teams, often comprised of multiple disciplines.

Benefits

  • Continuous learning & development opportunities
  • All your information will be kept confidential according to EEO guidelines.
  • Entrepreneurial journey.
  • Support with achieving professional development goals through guidance and real-time feedback.

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