Clinical Project Manager - 173876

ZP Group; United States; Remote; USD 140,000 - 170,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401(k)

Paid Time Off

Company-sponsored benefits

Job summary

Piper Companies is seeking a Project Manager to join a growing Clinical Research Organization supporting global clinical development programs. The Project Manager will oversee the execution of clinical trials from startup through closeout, serving as the primary liaison between sponsors and internal study teams while driving project timelines, quality, and financial performance.

The role requires 4+ years of clinical research experience, strong knowledge of ICH-GCP, and demonstrated ability to

Qualifications

• 4+ years of clinical research experience with exposure to multiple phases of clinical trials.
• Strong knowledge of ICH-GCP guidelines, regulatory requirements, and CRO operations.
• Experience managing project timelines, budgets, vendors, and cross-functional stakeholders.

Responsibilities

• Be the primary liaison for sponsors and internal study teams; provide study updates and address risks and issues.
• Lead cross-functional teams across Clinical Operations, Regulatory, Data Management, Safety, and external vendors to deliver studies.
• Oversee study timelines, plans, enrollment progress, site performance, and milestones from startup through closeout.
• Manage project budgets, forecasting, resource allocation, and change orders to support profitability and client objectives.
• Ensure compliance with ICH-GCP, protocol requirements, regulatory standards, and audit/inspection readiness.

Skills

Communication

Leadership

Problem-solving

Organization

Education

Bachelor's degree in Life Sciences/Clinical Research/Nursing

Job description

Piper Companies is seeking a Project Manager to join a growing Clinical Research Organization supporting global clinical development programs. The Project Manager will oversee the execution of clinical trials from startup through closeout, serving as the primary liaison between sponsors and internal study teams while driving project timelines, quality, and financial performance.

Responsibilities of the Project Manager include:

• Serve as the primary contact for clients, providing study updates, managing expectations, and proactively addressing project risks and issues.
• Lead cross-functional teams across Clinical Operations, Regulatory, Data Management, Safety, and external vendors to ensure successful study delivery.
• Oversee study timelines, project plans, enrollment progress, site performance, and operational milestones from startup through closeout.
• Manage project budgets, forecasting, resource allocation, and change orders to support project profitability and client objectives.
• Ensure compliance with ICH-GCP, protocol requirements, regulatory standards, and audit/inspection readiness throughout the study lifecycle.

Qualifications for the Project Manager include:

• Bachelor's degree in Life Sciences, Clinical Research, Nursing, or a related field.
• 4+ years of clinical research experience with exposure to multiple phases of clinical trials.
• Strong knowledge of ICH-GCP guidelines, regulatory requirements, and CRO operations.
• Experience managing project timelines, budgets, vendors, and cross-functional stakeholders.
• Excellent communication, leadership, problem-solving, and organizational skills.

Compensation for the Project Manager:

• Salary Range: $140,000 - $170,000
• Comprehensive Benefits: Medical, Dental, Vision, 401(k), Paid Time Off, and additional company-sponsored benefits.

This job opens for applications on 9/25/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: project manager, clinical research, CRO, clinical trials, clinical operations, ICH-GCP, regulatory compliance, study startup, site management, vendor management, project planning, risk management, budget management, resource allocation, forecasting, CTMS, eTMF, patient recruitment, study oversight, data management, pharmacovigilance, audit readiness, inspection readiness, stakeholder management, protocol review, regulatory submissions, clinical development, trial management, biotechnology, pharmaceutical industry, quality assurance, project leadership.

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