About the job
Senior Project Manager, Clinical Trials – REMOTE (U.S. Based)
Global CRO | Neuroscience-Focused | Permanent Role
Base: $125K–$140K + 401k Match + Full Benefits
The Opportunity:
We’re working with a global, tech-enabled CRO that’s transforming the way cognitive function is measured in clinical research and healthcare. With their digital assessment platform deployed in over 150 countries and across 2,000+ clinical trials, this organization is at the forefront of accelerating breakthroughs in neurology and brain health.
They’re hiring a Senior Project Manager with strong clinical trial experience to oversee complex, multinational studies and internal innovation projects. This is a strategic, client-facing role that blends traditional project management with exposure to digital health tools, cross-functional collaboration, and clinical operations leadership.
If you’ve led full-service studies, enjoy managing high-profile sponsor portfolios, and thrive in an agile, mission-driven environment—this could be a perfect fit.
Role Highlights:
- Own and lead the delivery of global clinical trials from Start-Up through Close-Out.
- Act as the primary sponsor point of contact, managing both individual studies and broader portfolios.
- Coordinate across internal teams (tech, ops, clinical, data science) to ensure on-time, on-budget delivery.
- Proactively identify and manage risks, solve problems, and guide teams through challenges.
- Oversee project financials: forecasting, invoicing, budget tracking, and change orders.
- Support proposal development for key accounts and work closely with business development.
- Drive internal innovation by leading process improvement initiatives and technology rollouts.
- Mentor junior team members and potentially step into line management responsibilities.
- Represent the company at investigator meetings and support sponsor audits as needed.
Ideal Candidate:
- 7+ years of clinical project management experience within a CRO, biotech, or pharmaceutical environment.
- Strong working knowledge of the drug development lifecycle and regulatory expectations.
- Bachelor’s degree in a scientific, technical, or healthcare field (e.g., Psychology, Biology, Nursing). Master’s or PMP certification a plus.
- Proven ability to manage global, multi-phase trials and engage cross-functional teams.
- Comfortable with Agile methodologies, digital health technologies, and clinical operations.
- Excellent communication and stakeholder management skills, including issue resolution.
- Experienced in project budgeting, invoicing, and financial oversight.
- Previous supervisory or mentorship experience preferred.
What’s In It For You:
- Remote-first flexibility across the U.S.
- High-impact role with real influence on patient outcomes and clinical innovation.
- Diverse global team working at the intersection of science, data, and technology.
- Culture focused on collaboration, continuous learning, and real-world impact.
Compensation & Benefits:
- Base Salary: $125,000 – $140,000 USD
- 401(k) match up to 3%
- Comprehensive medical, dental & vision benefits (plus free vision)
- 100% employer-paid short- and long-term disability & life insurance
- 30 days of total PTO (20 vacation, 10 personal) + 10 paid holidays
- Learning & development support for certifications, upskilling, and mentorship
This is a rare opportunity to join a purpose-driven, neuroscience-focused CRO that blends clinical rigor with innovation. If you’re a senior-level PM ready to take ownership of global studies and make a lasting impact—let’s talk.