Position Details
Sr Clinical Project Manager Apply
Job Description
Senior Clinical Project Manager
Location: Onsite – Pennington, NJ Hybrid
Step into a high-impact role where your work directly shapes the future of innovative therapies for rare and serious diseases. My client is advancing a cutting-edge clinical pipeline, and this role sits at the center of translating bold science into meaningful patient outcomes. You’ll lead complex global trials while influencing how clinical operations scale and evolve.
Why You Should Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19719.
Location: Onsite – Pennington, NJ Hybrid
Step into a high-impact role where your work directly shapes the future of innovative therapies for rare and serious diseases. My client is advancing a cutting-edge clinical pipeline, and this role sits at the center of translating bold science into meaningful patient outcomes. You’ll lead complex global trials while influencing how clinical operations scale and evolve.
Why You Should Apply
- Drive end-to-end clinical trials that can redefine standards of care
- Play a visible role partnering with senior leadership and key stakeholders
- Lead CROs, vendors, and cross-functional teams with real decision-making authority
- Contribute to building systems, SOPs, and operational excellence from the ground up
- Competitive salary range and bonus!
- Comprehensive benefits and growth-focused environment
- Lead clinical trials from protocol development through closeout
- Own project plans, timelines, budgets, and risk mitigation strategies
- Manage CROs, vendors, sites, and investigator relationships
- Ensure inspection readiness, regulatory compliance, and data integrity
- Optimize patient recruitment, retention, and operational performance
- Provide mentorship and leadership across clinical teams
- Bachelor’s degree in life sciences, pharmacy, nursing, or related field (advanced degree preferred)
- Strong knowledge of GCP, ICH, FDA, and EMA requirements
- Expertise with CTMS, EDC, and clinical trial systems
- Financial and vendor management acumen
- Confident leader in fast-paced, multi-study environments
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19719.
