Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.

Senior Clinical Project Manager – Oncology/Hematology, Phase III

Clinical OperationsClinical OperationsFull TimeRemoteTeam 10,001+H1B SponsorCompany SiteLinkedIn

Location

Arizona + 4 moreAll locations: Arizona, Maine, North Carolina, Ohio, Rhode Island

Posted

33 days ago

Salary

Not specified

Bachelor DegreeEnglishGoogle Cloud Platform

Job Description

• Drive the operational and financial success of Phase III clinical trials • Lead cross-functional teams across Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Medical Affairs, Pharmacovigilance, and QA • Act as the primary liaison with clients, ensuring smooth project launch, conduct, and closeout • Oversee project deliverables, timelines, and budgets while proactively identifying and mitigating risks • Mentor junior project managers and project support staff, fostering collaboration and professional growth • Own project budgets, forecasts, and financial performance • Ensure alignment and accountability across all vendors and study partners • Implement contingency plans and risk mitigation strategies to keep projects on track • Maintain and evaluate project progress using advanced tracking tools • Prepare and present project materials for internal and external stakeholders • Support inspection readiness and Trial Master File compliance • Participate in bid defense meetings as the potential project lead • Build strong client relationships to generate new opportunities • Stay up-to-date on oncology/hematology trends and the evolving drug development landscape • Train and mentor new project managers and clinical staff • Facilitate team communication, collaboration, and professional development

Job Requirements

  • Experienced Global Project Leader (NA, LATAM, EMEA, and APAC) with strong Phase III CRO project management experience
  • Oncology and Hematology expertise, with direct experience leading complex Phase III trials
  • Cross-functional team leadership, overseeing teams such as Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Medical Affairs, Pharmacovigilance, and Quality Assurance
  • Financially savvy, skilled in managing multi-million-dollar budgets, including creation, forecasting, and negotiation of out-of-scope work
  • Vendor management expertise, ensuring alignment, quality, and accountability across all study partners
  • Deep regulatory knowledge, with expertise in GCP/ICH guidelines and other applicable regulatory requirements
  • Educational foundation: Bachelor’s degree in Life Sciences, Medicine, Pharmacy, Nursing, or a related field
  • Tech-forward, comfortable leveraging digital tools and emerging technologies to optimize project delivery
  • Strategic, results-driven leader with exceptional communication skills, able to navigate complex, dynamic environments while inspiring teams to achieve excellence.

Benefits

  • Company car or car allowance
  • Health benefits to include Medical, Dental and Vision
  • Company match 401k
  • Eligibility to participate in Employee Stock Purchase Plan
  • Eligibility to earn commissions/bonus based on company and individual performance
  • Flexible paid time off (PTO) and sick time

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