Clinical Project Manager - Oncology; Client Dedicated​/Remote

Job Title

Clinical Project Manager - Oncology (Client Dedicated/Remote)

Sponsor Dedicated | Remote – United States

• Support and partner with Clinical Study Leads and cross‑functional study teams on global oncology trials
• Lead day‑to‑day study management activities across study startup, conduct, maintenance, and closeout
• Manage study timelines, deliverables, risks, and issue resolution
• Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers
• Coordinate Clinical Trial Team (CTT) meetings and drive action item follow‑up
• Support study‑level planning, forecasting, and operational strategy execution
• Monitor study performance metrics and proactively identify areas requiring intervention
• Ensure inspection readiness and compliance with applicable regulations and sponsor requirements
• Collaborate with stakeholders across Clinical Operations, Data Management, Biostatistics, Medical Monitoring, Regulatory Affairs, Safety, Supply Chain, and Quality
• Contribute to study status reporting and executive‑level communications
• Support achievement of study milestones, enrollment targets, database locks, and study closeout activities

• Bachelor's degree in a scientific, healthcare, or related field
• 3+ years of Clinical Project Management experience supporting global oncology clinical trials
• Experience managing studies across multiple countries and regions (North America, Europe, Asia‑Pacific, Latin America, or other global regions)
• Vendor management experience
• Strong understanding of clinical trial operations and study lifecycle management
• Experience supporting Phase I, II, III, and/or IV oncology studies
• Strong working knowledge of ICH‑GCP guidelines and clinical research regulations
• Proficiency with Microsoft Office Suite
• Ability to work effectively within global, cross‑functional matrix organizations

• Lung cancer (NSCLC, SCLC)
• Melanoma
• Renal cell carcinoma (kidney)
• Bladder cancer
• Head & neck squamous cell carcinoma
• Triple‑negative breast cancer
• Cervical cancer
• Gastric and gastroesophageal cancers
• Esophageal cancer
• Hepatocellular carcinoma (liver)
• Endometrial cancer
• Ovarian cancer
• Colorectal cancer
• Biliary tract cancer
• Prostate cancer
• Urothelial carcinoma
• Hematologic malignancies (multiple myeloma, lymphoma, leukemia)
• Antibody‑drug conjugates (ADCs)
• Personalized cancer vaccines
• KRAS inhibitors
• T‑cell engagers
• Cell‑directed immunotherapies

• Experience independently leading global oncology studies
• Experience supporting complex, multi‑regional Phase II and Phase III programs
• Experience with early‑phase oncology studies (Phase I/Ib)
• Experience with immuno‑oncology, targeted therapies, cell therapy, or hematologic malignancies
• Familiarity with CTMS, eTMF, IRT/RTSM, and clinical data review platforms
• Experience working in sponsor‑dedicated or FSP environments

• Strong project management and organizational skills
• Excellent communication and stakeholder management abilities
• Proven ability to manage multiple priorities in a fast‑paced environment
• Strong risk identification and mitigation capabilities
• Detail‑oriented with a focus on quality, compliance, and execution
• Strong collaboration skills across global teams and functions
• Ability to influence without direct authority and drive accountability across study teams

• Phase I / First‑in‑Human Studies
• Phase I/Ib Dose Escalation Studies
• Phase II Proof‑of‑Concept Studies
• Phase II/III Registrational Studies
• Phase III Global Pivotal Trials
• Phase IV and Post‑Marketing Studies

Salary Range: $120,000 – $135,000

Benefits may include a company car or car allowance, health benefits (medical, dental, vision), company match 401k, eligibility to participate in Employee Stock Purchase Plan, commissions/bonus based on performance, flexible paid time off (PTO) and sick time, and compliance with paid sick time requirements.

This posting is intended for an upcoming opportunity rather than a live role. By expressing your interest, you will be added to our talent pipeline and considered if the role becomes available.