Clinical Trials Supply Chain Manager

Park Street People; Uxbridge; On-site; GBP 80,000 - 100,000; Full time

Job summary

A global pharmaceutical company is seeking a Clinical Trials Supply Chain Manager to oversee the supply management for clinical trials in Uxbridge. This role is offered on a full-time, hybrid basis for 6 months. Candidates should have experience in clinical development, knowledge of regulatory compliance, and strong communication skills. This position involves ensuring timely and cost-effective management of clinical supplies, and remote applications will be considered.

Qualifications

• 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 studies efficiently.
• Create clinical development timelines and identify issue strategies.
• Liaise with external vendors and ensure product compliance.

Skills

Clinical supply management

Regulatory compliance

Communication skills

Analytical skills

Tools

IRT systems

CTMS systems

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.

Key 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

Requirements

• 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 age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.