Senior Clinical Project Manager Full Time

This role offers the opportunity to lead complex, high-impact clinical research projects across global and regional studies within a fast-growing, quality-driven clinical research environment. You will oversee end-to-end project execution across multiple phases of clinical trials, ensuring alignment between sponsors, internal teams, and external vendors. Acting as a key point of coordination, you will guide cross-functional teams through study start-up, execution, and close-out while ensuring timelines, budgets, and regulatory requirements are met. The position combines strategic oversight with hands-on project leadership, including risk management, financial tracking, and client communication. You will work closely with scientific, operational, and regulatory stakeholders to drive study success and operational excellence. This is a highly visible role where your leadership directly influences clinical outcomes and client satisfaction.

Accountabilities

• Lead the planning, execution, and delivery of Phase I-IV clinical trials, ensuring alignment with contractual scope, timelines, budgets, and regulatory requirements.
• Coordinate cross-functional teams including clinical operations, data management, biostatistics, regulatory, and vendors to ensure seamless project execution.
• Develop and maintain detailed project plans, including resource allocation, financial tracking, risk assessment, and mitigation strategies.
• Monitor project performance, track progress against milestones, and provide regular status updates to internal leadership and external sponsors.
• Manage client relationships, acting as the primary point of contact for project communication, issue resolution, and change order discussions.
• Ensure compliance with ICH guidelines, FDA, Health Canada, EMA, and other applicable regulatory standards throughout the project lifecycle.
• Identify and escalate project risks, resource gaps, or scope changes while ensuring timely corrective actions and resolution.

Requirements

• Bachelor’s or Master’s degree in Life Sciences, Health Sciences, or a related field.
• 10+ years of experience in clinical research and development within a pharmaceutical, biotechnology, or CRO environment.
• At least 7 years of direct clinical project management experience across multiple phases of clinical trials.
• Strong knowledge of clinical trial processes including site selection, study start-up, monitoring, data management, regulatory submissions, and vendor management.
• Oncology clinical trial experience is required.
• Solid understanding of global regulatory frameworks including ICH, FDA, Health Canada, and EMA guidelines.
• Strong financial acumen with experience in budgeting, forecasting, and managing project profitability.
• Excellent leadership, communication, negotiation, and stakeholder management skills.
• Strong problem-solving abilities with the capacity to manage conflict and drive resolution in complex environments.
• Willingness to travel up to 20%, including internationally when required.

Benefits

• Competitive salary range of $125,000 to $175,000 annually.
• Comprehensive medical, dental, and vision insurance coverage.
• Life, AD&D, short-term, and long-term disability insurance.
• 401(k) retirement savings plan.
• Generous paid time off and sick leave policy.
• Tuition reimbursement and fitness reimbursement programs.
• Employee assistance program (EAP) supporting well-being and mental health.
• Performance-based bonus opportunities.
• Remote-friendly work arrangement within the United States.

How Jobgether Works

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role’s core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

Why Apply Through Jobgether?

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