Project Manager

Verbatim Pharma; Amsterdam; Hybrid; EUR 70,000 - 95,000; Full time

Benefits offered by this job

Join international organisation

Global clinical trial projects

Cross-functional collaboration

Development and progression

Job summary

Verbatim Pharma in Amsterdam is seeking a Clinical Supply Project Manager to lead multiple global clinical trial projects in a hybrid work setting. You will liaise with clients, coordinate timelines, and drive deliverables across cross-functional teams to ensure regulatory and quality standards are met.

The role demands 2+ years in pharma or clinical supplies, strong organisational and communication skills, and the ability to manage several projects in a fast-paced environment.

Qualifications

• Minimum 2+ years within pharmaceuticals, clinical supplies or related industry.
• Strong project management and organisational skills.
• Experience in a client-facing environment.
• Understanding of GMP and regulated environments.
• Strong communication and stakeholder management skills.
• Ability to manage multiple projects in a fast-paced environment.

Responsibilities

• Manage multiple clinical supply projects from start to finish.
• Act as a key point of contact for clients.
• Coordinate project timelines, deliverables and requirements.
• Work closely with internal teams and external partners.
• Identify potential risks and provide solutions.
• Ensure projects are delivered in line with quality and regulatory requirements.

Skills

Project management

Organisational skills

Client facing

GMP knowledge

Communication

Stakeholder management

Job description

Clinical Supply Project Manager | Clinical Services | Amsterdam Region | Hybrid

Are you an experienced Project Manager with a background in pharmaceuticals or clinical trials looking for your next opportunity?

What’s in It for You

• Join a growing, international organisation
• Work on a variety of global clinical trial projects
• Collaborate with cross-functional and international teams
• Strong opportunities for development and progression

What You’ll Be Doing

• Manage multiple clinical supply projects from start to finish
• Act as a key point of contact for clients
• Coordinate project timelines, deliverables and requirements
• Work closely with internal teams and external partners
• Identify potential risks and provide solutions
• Ensure projects are delivered in line with quality and regulatory requirements

What We’re Looking For

• 2+ years’ experience within pharmaceuticals, clinical supplies or a related industry
• Strong project management and organisational skills
• Experience working in a client-facing environment
• Understanding of GMP and regulated environments
• Strong communication and stakeholder management skills
• Ability to manage multiple projects in a fast-paced environment

Location: Netherlands

Working Model: Hybrid

If you’re a proactive, solutions-focused Project Manager looking to develop your career within the clinical trial industry, we’d love to hear from you!