5 часов назад
Sr. Clinical Trial Manager, Therapeutics and Oncology
130 800 - 209 400$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Sr. Clinical Trial Manager, Therapeutics and Oncology (clinical trial management): Overseeing complex therapeutic and oncology clinical trials across multiple regions with an accent on vendor management, study timelines, clinical data review, and ICH/GCP compliance. Focus on leading cross-functional trial teams, managing CRO oversight and feasibility, and ensuring quality, budget, and delivery milestones.
Location: Princeton, New Jersey, United States; hybrid 70/30 work model with 70% in-office collaboration. Only U.S. persons are eligible due to U.S. export control requirements.
Salary: $130,800–$209,400 per year, with potential eligibility for an annual discretionary bonus, incentive compensation, or equity award.
Company
develops mRNA-based medicines and technologies for transforming how medicines are created and delivered.
What you will do
- Manage and oversee assigned clinical trials across all phases, ensuring quality, compliance, timelines, and deliverables.
- Lead clinical trial teams and represent Clinical Operations on cross-functional development teams.
- Manage CRO and vendor oversight, trial feasibility, site capability assessments, monitoring reports, and study-level documentation.
- Review clinical data, quality metrics, deviations, study systems, and trial samples to support data review and operational readiness.
- Manage study timelines, budgets, invoices, forecasting, dashboards, and status reporting for senior management.
- Support clinical documents, operational workstreams, continuous improvement initiatives, and collaborative stakeholder relationships.
Requirements
- 5–7 years of experience in clinical research and the pharmaceutical or biotechnology industry, including at least 2 years of independent trial management.
- Bachelor’s degree required; advanced degree preferred.
- Robust oncology and rare disease experience required; immuno-oncology and high-complexity experience such as CAR-T are desirable.
- Strong understanding of drug development, project management, FDA requirements, and ICH/GCP guidelines.
- Excellent verbal and written communication, organizational skills, and attention to detail.
- Must qualify as a U.S. person and be able to access export-controlled information; visa sponsorship is not available.
Culture & Benefits
- 70/30 in-office work model supporting collaboration, teamwork, and mentorship.
- Healthcare and voluntary benefits programs.
- Fitness, mindfulness, mental health, and broader well-being resources.
- Family planning benefits, including fertility, adoption, and surrogacy support.
- Paid time off including vacation, volunteer days, sabbatical, global recharge days, and year-end shutdown.
- Savings and investment programs, plus location-specific perks.
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