Clinical Supplies Manager

Park Street People; London; Hybrid; GBP 45,000 - 60,000; Full time

Job summary

A global pharmaceutical company is seeking a Clinical Supply Chain Manager in Uxbridge for a 12-month, full-time role. The individual will oversee clinical supplies management for trials and drug development, ensuring prompt and cost-effective delivery. This hybrid position allows for remote applications, inviting applicants with a strong pharmaceutical background and an analytical mindset.

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 in a timely manner.
• Create clinical development timelines and identify strategies for issues.
• Act as the clinical supplies point of contact with external vendors.

Skills

Clinical development

Communication

Analytical skills

Tools

IRT systems

CTMS systems

Job description

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Our client, a global pharmaceutical company, is currently looking for a Clinical Supply Chain Manager to join their team in Uxbridge on a full time, 12-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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science and Supply Chain

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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