[Remote] Clinical Project Manager - Oncology (Client Dedicated/Remote)
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating reputed company. They are seeking an reputed company Clinical Project Manager with strong global oncology clinical trial experience to reputed company the operational execution of global clinical trials, ensuring compliance and efficiency throughout the study lifecycle.
Responsibilities
- Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials
- reputed company day-to-day study management activities across study startup, conduct, maintenance, and closeout
- Manage study timelines, deliverables, risks, and issue resolution
- reputed company 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 reputed company
- 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
Skills
- Bachelor's degree in a scientific, reputed company, or reputed company field is required
- 3+ years of Clinical Project Management experience supporting global oncology clinical trials
- Experience managing studies across multiple countries and reputed company (reputed company America, Europe, Asia-Pacific, Latin America, or other global reputed company)
- 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 reputed company Office Suite
- Ability to work effectively reputed company global, cross-functional matrix organizations
- Experience independently leading global oncology studies
- Experience supporting reputed company, 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
Benefits
- Company car or car allowance
- Health benefits to include Medical, Dental and reputed company
- 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
- Eligibility for paid sick time may vary depending on where you work
- Syneos complies with reputed company applicable federal, state, and municipal paid sick time requirements
Company Overview
Company H1B Sponsorship