Application

Our Clinical Project Management (CPJM) team plays a vital role in delivering high-quality clinical projects, including commercially sponsored clinical trials, while supporting the development of Perspectum’s innovative products and services.

About The Role

The Clinical Project Manager I – Logistics & Sample Management role combines clinical project coordination with hands-on responsibility for trial sample logistics. The role sits within the CPJM team and supports the delivery of clinical trials, with a primary focus on ensuring the efficient, compliant, and timely management of biological sample shipments across international sites. 
 
Approximately 50% of the role focuses on sample management and logistics, with the remainder supporting broader clinical project management activities across a portfolio of trials. 

The CPJM team manages and delivers clinical projects requiring a strong understanding of the clinical trial process. This role builds on that foundation, integrating operational logistics ownership. 
 
About You

- Lead the end-to-end coordination of sample shipments globally, ensuring compliance with regulatory and GCP requirements 
- Support day-to-day clinical project operations, working closely with internal teams to ensure smooth study delivery 
- Act as a key operational link between sites, couriers, CROs, and internal stakeholders 
- Contribute to continuous improvement of logistics and project delivery processes 
 
This is a hands-on, fast-paced role requiring strong organisational skills, proactive problem-solving, and the ability to manage competing priorities. This role is particularly suitable for a self-motivated team player who is comfortable with managing multiple stakeholders. 

You will:

• Manage end-to-end coordination of international sample shipments, ensuring compliance with GCP and regulatory standards
• Maintain accurate tracking and chain-of-custody records for all samples 
• Liaise with clinical sites, couriers, and central labs to plan and execute shipment
• Support CPJM team with study management and day-to-day operations 

Experiance 

• Experience in clinical trials, logistics, or sample management 
• Strong organisational and problem-solving skills 
• Excellent communication skills (written and verbal) 
• Ability to manage multiple priorities under pressure  
• Proficiency in Microsoft Office 

About Us

All our benefits information can be found in the downloadable Benefits document under 'Information' on the right hand side of this screen.

At Perspectum, we are committed to fostering diversity, equity, and inclusion. We prioritise hiring based on merit, skills, and qualifications, valuing individuals for their unique contributions while ensuring a culture that respects and celebrates differences. If you require any reasonable adjustments as part of your application process, please let our Talent Team know.