Senior Clinical Project Leader – Global Trials (Hybrid/Remote)

Allucent; Lombardia; Hybrid; EUR 70.000 - 110.000; Vollzeit

Benefits dieser Stelle

Flexible Working hours

Remote/office flexibility depending on

Buddy Program

Training budget for development

Internal growth opportunities

Employee referral program

Zusammenfassung

Allucent is seeking a Senior Project Manager to lead clinical trials across Oncology, Neuroscience, Immunology and Infectious Diseases with a focus on start-up to close-out delivery. You will oversee study budgets, vendor management, RM, quality, and regulatory compliance, working with sponsor teams and cross-functional groups in a hybrid/remote setting.

The role requires a life science, healthcare or business degree, at least 5 years in drug development or clinical research and strong

Qualifikationen

• Requires a minimum Bachelor’s degree in life science, healthcare and/or business.
• At least 5 years of relevant work experience in drug development or clinical research.
• Expert knowledge of ICH-GCP(R2), data privacy practices, and regulatory requirements.
• Strong financial acumen, administrative excellence and analytical skills.

Aufgaben

• Leads the project team and ensures delivery within scope and timelines.
• Develops and executes project management plans per established processes.
• Manages study budget, invoicing, and vendor relationships.
• Ensures quality and adherence to GCP, SOPs, and regulatory guidelines.
• Maintains Trial Master File and serves as primary sponsor-team liaison.

Kenntnisse

Project management

Leadership

Communication

Financial acumen

Problem solving

English proficiency

Regulatory knowledge

Ausbildung

Bachelor's degree in life science, healthcare and/or business

Tools

MS Word

MS Excel

MS PowerPoint

MS Project

Jobbeschreibung

Allucent is seeking a Senior Project Manager to lead clinical trials across Oncology, Neuroscience, Immunology and Infectious Diseases with a focus on start-up to close-out delivery. You will oversee study budgets, vendor management, RM, quality, and regulatory compliance, working with sponsor teams and cross-functional groups in a hybrid/remote setting.

The role requires a life science, healthcare or business degree, at least 5 years in drug development or clinical research and strong