CLINICAL PROJECT MANAGER II - ONCOLOGY Sponsored dedicated, Remote - United States
Overview As a Clinical Project Manager II, you will play a critical role in the operational leadership and execution of global oncology clinical trials. You will support a high‑performing sponsor‑dedicated team across multiple indications and phases, ensuring studies are conducted efficiently, compliantly, and within established timelines.
Key Responsibilities 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
Required Qualifications 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 required
Strong understanding of clinical trial operations and study lifecycle management
Experience supporting Phase I, Phase II, Phase III, and/or Phase 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
Oncology Therapeutic Area Experience Solid Tumors
Non‑Small Cell Lung Cancer (NSCLC)
Small Cell Lung Cancer (SCLC)
Breast Cancer
Ovarian Cancer
Cervical Cancer
Endometrial Cancer
Prostate Cancer
Colorectal Cancer
Pancreatic Cancer
Gastric Cancer
Esophageal Cancer
Hepatocellular Carcinoma (HCC)
Melanoma
Renal Cell Carcinoma (RCC)
Bladder Cancer
Head and Neck Cancer
Thyroid Cancer
Sarcoma
Gynecologic Malignancies
Hematologic Malignancies
Multiple Myeloma
Acute Myeloid Leukemia (AML)
Acute Lymphoblastic Leukemia (ALL)
Chronic Lymphocytic Leukemia (CLL)
Chronic Myeloid Leukemia (CML)
Hodgkin Lymphoma
Non‑Hodgkin Lymphoma
Myelodysplastic Syndromes (MDS)
Myeloproliferative Neoplasms (MPN)
Preferred Qualifications 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
Key Skills & Competencies 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
Clinical Phase Experience We welcome candidates with experience supporting 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. Experience supporting global, multi‑country oncology programs through multiple phases of development is highly preferred.
Salary Range $120,000 - $135,000
Equal Opportunity Statement 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.
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