- Location
- United States · published
- Type
- Full-time
- Department
- IT
- Seniority
- Manager
- Source
- Workable
Description
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
Looking to take your project management expertise to the next level? Join us as a Project Manager II (PM II) and lead the delivery of complex clinical trials that make a meaningful impact for patients worldwide. We are seeking a strategic and execution-focused leader with strong experience managing Infectious Disease, Immunology & Inflammation, Cell & Gene Therapy, and Neurology who thrives in a fast-paced, collaborative environment.
About the Role
As a Project Manager II, you will lead with impact and drive global clinical trials from study start-up through final delivery. You’ll oversee cross-functional teams, ensuring studies remain on track, on budget, and compliant with GCP and regulatory requirements while serving as the primary point of contact for sponsors, vendors, and internal stakeholders. With a focus on proactive problem-solving, risk mitigation, and operational excellence, you’ll play a critical role in delivering high-quality clinical programs that exceed client expectations.
Your main responsibilities will include but not limited to:
- Driving project success by leading cross-functional teams to deliver clinical trials on time, within scope, and on budget.
- Ensuring excellence and compliance by developing and executing project plans aligned with GCP, SOPs, and regulatory standards.
- Aligning stakeholders by serving as the primary point of contact for sponsors, vendors, and internal teams.
- Optimizing vendor performance through strategic selection, management, and oversight.
- Mitigating risks and control budgets by proactively addressing challenges, scope changes, and resource allocation.
- Maintaining inspection-ready documentation by leading key meetings and ensuring the Trial Master File and study records are complete.