Sr Clinical Project Manager

International Erosion Control Association; Northern (KY); Hybrid; USD 120,000 - 160,000; Full time

Job summary

International Erosion Control Association is seeking a Senior Clinical Project Manager in Pennington, NJ (hybrid) to lead global trials from protocol development through closeout, translating bold science into meaningful patient outcomes.

You will own project plans, timelines, budgets and risk mitigation, manage CROs, vendors and investigator relationships, ensure inspection readiness and data integrity, and mentor cross-functional clinical teams.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Strong knowledge of GCP, ICH, FDA, and EMA requirements.
• Experience with CTMS and EDC systems.
• Financial and vendor management acumen.
• Leadership in fast-paced, multi-study environments.

Responsibilities

• 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.

Skills

GCP knowledge

FDA/EMA knowledge

Project management

Vendor management

Education

Bachelor’s degree in life sciences

Advanced degree preferred

Tools

CTMS

EDC

Job description

Senior Clinical Project Manager

Location: 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

What You’ll Be Doing

• 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

About You

• 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