About the Role
The role involves leading clinical trial projects from initiation through completion, managing timelines, resources, and stakeholder communication across multiple therapeutic areas.
Responsibilities
- Lead end-to-end execution of clinical trials across multiple phases
- Develop and manage project timelines, budgets, and resource allocation
- Coordinate activities between internal teams and external vendors
- Ensure compliance with regulatory requirements and quality standards
- Monitor trial progress and implement risk mitigation strategies
- Prepare and present project status reports to stakeholders
- Manage contract research organization (CRO) performance and deliverables
- Oversee clinical operations planning and site activation timelines
- Facilitate cross-functional team meetings and decision-making forums
- Drive adoption of best practices in project management methodologies
- Support protocol development and study design input
- Manage trial documentation including study plans and reports
- Ensure data integrity and timely database lock processes
- Collaborate with safety, biostatistics, and medical monitoring teams
- Lead project change control and scope management processes
Compensation
Competitive salary and comprehensive benefits package including performance incentives
Work Arrangement
Hybrid work model with partial remote flexibility based on location
Team
Part of a dedicated clinical operations group supporting diverse therapeutic areas
Why Join Us
- Opportunity to work on innovative therapies across oncology, immunology, and rare diseases
- Collaborative environment emphasizing professional growth and leadership development
- Exposure to cutting-edge trial designs and precision medicine applications
Travel Requirements
Up to 20% travel may be required for site visits, sponsor meetings, or team gatherings
Available for qualified candidates requiring sponsorship
