Senior Clinical Trial Lead — Hybrid/Remote

Allucent; Netherlands; Hybride; EUR 90 000 - 120 000; Plein temps

Avantages offerts par ce poste

Comprehensive benefits package per 위치

Flexible working hours

Remote/office working depending on loc

Internal growth opportunities and карь

Résumé du poste

Allucent is seeking a Sr. Project Manager to coordinate clinical trials across Oncology, Neuroscience, Immunology and Infectious Diseases. You will lead study teams, manage budgets and vendors, and ensure regulatory compliance throughout the lifecycle. Hybrid/remote work options available.

The role requires 5+ years in drug development or clinical research, with strong PM experience and excellent communication, planning and problem-solving skills. English proficiency is essential.

Qualifications

• Minimum 5 years of relevant work experience in clinical research or drug development.
• Minimum 5 years of experience in drug development and/or clinical research with at least 3 years PM.
• Excellent written and verbal communication and organizational skills.
• Strong financial acumen and ability to manage budgets and invoicing.

Responsabilités

• Leads the project team and ensures delivery according to scope and timelines.
• Creates and executes PM plans and ensures adherence to SOPs and GCP.
• Manages vendors, budgets, risks, and study documentation.
• Communicates with sponsor teams and maintains project progress reports.
• Oversees Trial Master File and acts as primary sponsor-contact point.

Connaissances

Project management

Stakeholder communication

Budget management

ICH-GCP(R2) knowledge

Clinical trial delivery

Formation

Bachelor’s degree in life sciences/healthcare/business

Outils

Microsoft Word

Excel

PowerPoint

Description du poste

Allucent is seeking a Sr. Project Manager to coordinate clinical trials across Oncology, Neuroscience, Immunology and Infectious Diseases. You will lead study teams, manage budgets and vendors, and ensure regulatory compliance throughout the lifecycle. Hybrid/remote work options available.

The role requires 5+ years in drug development or clinical research, with strong PM experience and excellent communication, planning and problem-solving skills. English proficiency is essential.