Project Director - Oncology

precisionmedicinegroup; EE. UU.; A distancia; USD 120.000 - 180.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Discretionary annual bonus

Health insurance

Retirement savings

Life and disability coverage

Parental leave

Paid time off

Descripción de la vacante

Precision Medicine Group seeks an experienced Senior Clinical Project Manager to direct complex global clinical research trials and a portfolio of studies, ensuring successful delivery, strong client service, financial performance, and quality assurance.

You will lead cross-functional teams and project managers, maintain inspection readiness, manage budgets and change orders, and drive process improvements that enhance execution and outcomes across programs.

Formación

• Bachelor’s degree or equivalent in science/health; advanced degree preferred.
• 8+ years of clinical research experience, with 5+ years in direct project management or equivalent.
• Experience managing complex global studies or a portfolio of studies.
• Proficient with MS Office, MS Project, eTMF, EDC, and CTMS.
• Excellent communication, organization, attention to detail, and client service.

Responsabilidades

• Serve as the main client contact, support proposals and presentations, and lead sponsor and internal project meetings.
• Oversee trial planning and delivery, guiding PMs through setup, procurement, execution, and closeout.
• Manage budgets, scope, profitability, billing, forecasting, and change orders; identify out-of-scope work early.
• Develop or oversee project plans, timelines, metrics, and risk, change, and mitigation strategies.
• Maintain quality and inspection readiness, address findings with corrective actions, and ensure study training is completed.
• Coordinate cross-functional teams, report progress and issues, mentor project staff, and support bid defense and process improvement activities.

Conocimientos

Communication

Organization

Attention to detail

Client service

Educación

Bachelor’s degree or equivalent in science/health field

Advanced degree preferred

Herramientas

Microsoft Office

Microsoft Project

Electronic Trial Master Files (eTMF)

Electronic Data Capture (EDC)

Clinical Trial Management System (CTMS)

Descripción del empleo

Role overview

Direct complex clinical research trials or a portfolio of studies, with responsibility for delivery, client service, financial performance, and quality. The role may oversee global or large-scale programs, guide project managers, and contribute to improvements in project execution and organizational processes.

Responsibilities

• Serve as the main client contact, support proposals and presentations, and lead sponsor and internal project meetings.
• Oversee trial planning and delivery, guiding project managers through setup, procurement, execution, and closeout.
• Manage budgets, scope, profitability, billing, forecasting, and change orders; identify out-of-scope work early.
• Develop or oversee project plans, timelines, metrics, and risk, change, and mitigation strategies.
• Maintain quality and inspection readiness, address findings with corrective actions, and ensure study-specific training is completed.
• Coordinate cross-functional teams, report progress and issues, mentor project staff, and support bid defense and process improvement activities.

Requirements

• Bachelor’s degree or equivalent education and experience in a science or health-related field; an advanced degree is preferred.
• At least eight years of clinical research experience, including five years in direct project management or equivalent demonstrated capability.
• Experience managing complex global studies or a portfolio of studies.
• Strong working knowledge of Microsoft Office, Microsoft Project, electronic trial master files, electronic data capture, and clinical trial management systems.
• Excellent communication, organization, attention to detail, and client service skills.
• Preferred: strong command of ICH-GCP, relevant operating procedures, project management methods, and cross-functional planning, risk, and change management.

Benefits and work setup

The source lists eligibility for a discretionary annual bonus, health insurance, retirement savings, life and disability coverage, parental leave, and paid sick and vacation time. Candidates must already be legally authorized to work in the country of employment without sponsorship.