Senior Clinical Project Manager: Hybrid/Remote

Allucent; Amsterdam; Ibrido; EUR 90.000 - 130.000; Tempo pieno

Vantaggi offerti da questo lavoro

Flexible working hours

Remote/office work depending on locale

Training and mentorship opportunities

Industry-leading benefits

Descrizione del lavoro

Allucent is seeking a Sr. Project Manager to coordinate clinical trials from start-up to delivery. The role focuses on oncology, neuroscience, immunology and infectious diseases, with cell and gene therapy experience a plus.

You will lead the project team, manage vendors, and ensure timelines, budgets, and regulatory requirements are met in a fast-paced environment. This hybrid/remote role offers flexible working arrangements.

Competenze

• Minimum Bachelor's degree in life science, healthcare and/or business.
• Minimum 5 years of relevant work experience.
• Minimum 5 years of experience in drug development and/or clinical research, with at least 3 years of clinical trial project management experience.
• Preference for candidates with CRA experience.
• Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and applicable regulatory requirements.
• Strong financial acumen, administrative excellence and analytical skills.
• Experience managing all phases of the full-service clinical trial delivery lifecycle (Start-up, Maintenance, Close-out).
• Excellent written and verbal communication, planning, critical thinking and organizational skills, including command of English language.
• Strong presentation skills and client-focused attitude.

Mansioni

• Leads the project team and ensures delivery according to scope and timelines.
• Creates and executes project management plans per established processes.
• Ensures quality and adherence to GCP, SOPs and regulatory guidelines.
• Establishes communication lines and escalation pathways with stakeholders.
• Oversees study documents and contributes to protocol and study reports.
• Manages training plans for project teams and vendor activities.
• Leads meetings with internal and sponsor teams, including KOMs and Investigator Meetings.
• Oversees vendor identification, qualification and management.
• Optimizes resource utilization across projects and programs.
• Prepares and circulates project progress and status reports.
• Manages the study budget and monthly invoicing.
• Implements risk management plans and handles scope changes.
• Maintains Trial Master File and ensures inspection readiness.
• Acts as primary point of communication between sponsor and team.

Conoscenze

Project management

GCP & regulatory knowledge

Communication skills

Financial acumen

English language

Clinical trial management

Formazione

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

Strumenti

MS Word

MS Excel

PowerPoint

Descrizione del lavoro

Allucent is seeking a Sr. Project Manager to coordinate clinical trials from start-up to delivery. The role focuses on oncology, neuroscience, immunology and infectious diseases, with cell and gene therapy experience a plus.

You will lead the project team, manage vendors, and ensure timelines, budgets, and regulatory requirements are met in a fast-paced environment. This hybrid/remote role offers flexible working arrangements.