With our focus on small and mid-size biopharma companies, project management takes on a prominent role in clinical operations. In addition to providing project oversight and governance, and bringing best-practice methodologies to trial conduct, our team takes a proactive approach to help you meet your objectives expeditiously. While our role largely entails project orchestration, keeping activities on track and ensuring accountability, we serve another essential function: anticipating potential challenges and risks and working in partnership with you to mitigate and provide solutions.
We believe projects are most successful when the customer and Allucent create a single, integrated project team. This allows the development of interdependent working relationships with a mutual sense of ownership and shared vision and respect.
Allucent has invested in project managers who are seasoned in managing complex initiatives and programs with deep therapeutic expertise and strong leadership experience that informs our approach. We are fearless in asking questions and challenging assumptions, an essential quality when working with creative minds on innovative and perhaps unconventional ideas. We act as guide and gatekeeper, helping you focus on the resources and infrastructure required to bring novel therapies to market.
Working with Allucent, you’ll find a responsive and nimble team that gets things done without layers of bureaucracy in the way. Your project benefits from a dedicated project manager, your single point of contact, supported by a project director, who will work with you from start to finish, including working with our consulting team. Robust escalation pathways are in place for problem-solving when necessary, with clear access to Allucent senior management when required.
For study management, our team works with the industry-leading Veeva Vault. The Vault Clinical Suite, encompassing Clinical Trial Management System (CTMS), eTMF, Study Start-Up, and more, delivers real-time visibility and oversight, accelerates and streamlines study execution, and improves collaboration and efficiency between study partners.
Key focus areas include:
- Efficient study startup
- Optimized balanced resourcing
- Strategic patient recruitment
- High-quality delivery of trial operations
- Risk-based quality management