Clinical Trials Supply Chain Manager

ZipRecruiter; Uxbridge; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading global pharmaceutical company based in Uxbridge is seeking a Clinical Trials Supply Chain Manager for a 6-month hybrid role. The successful candidate will oversee clinical supplies for trials, ensuring timely and cost-effective management while liaising with external vendors and complying with regulations. Strong experience in clinical development and project management is essential. This role offers flexibility with some remote working options.

Qualifications

• Previous experience in a clinical development role within a pharmaceutical setting.
• Strong knowledge of clinical supply and drug development processes.
• Understanding of global regulatory requirements.

Responsibilities

• Manage clinical supply strategies within clinical studies.
• Create clinical development timelines and proactively identify strategies.
• Act as the clinical supplies point of contact and liaise with external vendors.

Skills

Clinical supply management

Project management

Communication skills

Analytical skills

Tools

IRT systems

CTMS systems

Job description

Overview

Job Description

Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Manager to join their team in Uxbridge on a full time, 6-month temporary basis (35 hours per week).

This role is expected to be worked on a hybrid basis but remote applications will also be considered.

You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.

Responsibilities

• Manage clinical supply strategies within clinical studies whilst ensuring these delivered in a timely and cost-efficient manner
• Create clinical development timelines and proactively identify strategies and solutions for any issues that may arise
• Support the creation of medical protocols drafts and in the developing of package and label outlines
• Act as the clinical supplies point of contact and liaise with external vendors and services
• Ensure all products meet protocols and regulatory requirements

Qualifications

• Previous experience in a clinical development role within a pharmaceutical setting
• Strong knowledge of clinical supply and drug development processes
• Understanding of global regulatory requirements
• Previous experience in planning and managing clinical studies strategies
• Preferably, good knowledge of IRT and CTMS systems
• Excellent communication and analytical skills

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of , , , , creed or and comply with all relevant UK legislation.

We are acting as an Employment Business in relation to this role