Senior Clinical Project Manager - Oncology/Hematology (Phase III) Required (Remote - US/Canada)

Senior Clinical Project Manager – Oncology/Hematology (Phase III) (Remote – US/Canada) Are you a seasoned CRO project leader passionate about advancing oncology and hematology research? Do you thrive in a fast‑paced, collaborative environment where your leadership directly impacts patient outcomes? Join our team as a Senior Project Manager and take ownership of complex Phase III trials, driving projects from proposal through delivery and shaping the future of cancer care. About the Role As a Senior Project Manager, you will take a lead role in advancing Phase III oncology and hematology clinical trials, managing complex, global initiatives. You'll lead and inspire cross‑functional teams, mentor emerging project managers, and act as the primary strategic partner for our clients, ensuring every milestone is delivered on time, on budget, and with exceptional quality. What You’ll Do Project Leadership & Delivery 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. Financial & Operational Accountability 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. Reporting & Communication 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. Business Development 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. Management & Mentorship Train and mentor new project managers and clinical staff. Facilitate team communication, collaboration, and professional development. Who You Are Experienced Global Project Leader with strong Phase III CRO project management experience and a proven track record of delivering clinical trials successfully. 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 QA. Financial 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. Why You’ll Love Working Here Highly collaborative, innovative, and performance‑driven team. Opportunities to mentor and be mentored, helping you grow professionally while developing others. Work on impactful global oncology and hematology trials, shaping the future of patient care. Environment where innovation, growth, and professional development are actively encouraged. If you are ready to lead high‑impact Phase III oncology and hematology clinical trials, drive innovation, and make a real difference in patient outcomes, we want to hear from you! Salary Range The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr Syneos Health/ inVentiv Health Commercial LLC