[Remote] Clinical Project Manager - Oncology (reputed company 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 reputed company on accelerating reputed company. They are seeking a Clinical Project Manager II with strong global oncology clinical trial experience to reputed company operational execution and delivery of global oncology clinical trials.
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 reputed company
- reputed company external vendors, CROs, central laboratories, imaging vendors, and specialty providers
- Coordinate Clinical Trial Team (CTT) meetings and drive reputed company item follow-up
- Support study-level planning, forecasting, and operational reputed company 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 reputed company
- 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, Europe, Asia-reputed company, 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 reputed company 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
- A 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 reputed company time off (PTO) and reputed company time
- Because certain states and municipalities have regulated reputed company reputed company time requirements, eligibility for reputed company reputed company time may vary depending on where you work
- Syneos complies with reputed company applicable federal, state, and municipal reputed company reputed company time requirements
reputed company
Company H1B Sponsorship