Note: The job is a remote job and is open to candidates in USA. Novocure is a company focused on extending the lives of patients battling aggressive cancers. As a Clinical Trial Lead, you will oversee global clinical studies outsourced to CROs, ensuring successful delivery while managing cross-functional teams, timelines, and budgets.
Responsibilities
- Lead cross-functional Clinical Study Teams from study startup through closeout
- Serve as the primary liaison between Novocure and CRO partners
- Oversee study timelines, milestones, deliverables, and risk mitigation plans
- Manage study budgets, change orders, invoices, and financial performance
- Monitor CRO and vendor performance to ensure quality and compliance
- Support protocol development, feasibility assessments, and study planning
- Track KPIs and proactively resolve operational challenges
- Support database lock, clinical study reports, audits, inspections, and regulatory submissions
- Partner with global colleagues across North America, Europe, and Israel
Skills
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field
- 5–7+ years of clinical research experience, including 2–3+ years leading global clinical studies
- Experience leading studies from startup through closeout
- Experience managing CROs, vendors, study budgets, and project timelines
- Strong knowledge of ICH-GCP, FDA, EMA, and global regulatory requirements
- Excellent leadership, communication, and project management skills
- Oncology clinical trial experience strongly preferred
- Experience leading other highly complex global studies
- Experience with CTMS, eTMF, and EDC systems
- Advanced degree (MS, PharmD, or PhD)
Benefits
- Annual incentive bonus
- Restricted stock unit grant
- A full range of benefits
Company Overview