Clinical Supply Planner

JR United Kingdom; Preston; Hybrid; GBP 40,000 - 70,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Clinical Supply Planner to manage the supply chain for clinical trials. This key role involves coordinating with various stakeholders, ensuring regulatory compliance, and optimizing processes within a hybrid working environment. Ideal candidates will have strong experience in pharmaceutical supply chain management and excellent communication skills.

Benefits

Hybrid working environment with flexibility

Pension

Life insurance

Annual leave

Performance bonus

Qualifications

• Experience in clinical trials across multiple territories and sites.
• Knowledge of regulatory compliance and documentation.
• Strong stakeholder engagement and communication skills.

Responsibilities

• Manage clinical demand and coordinate with teams to meet supply needs.
• Maintain documentation and SOPs for clinical supply chain activities.
• Oversee inventory, shipments, and regulatory compliance.

Skills

Pharmaceutical supply chain management

Stakeholder management

Communication skills

Education

Experience with GXP, GCP, GMP

Knowledge of ERP systems

Job description

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Clinical Supply Planner, Preston, Lancashire

Essential Pharma is seeking a Clinical Supply Planner to join our team in Preston, Lancashire, UK. The role involves managing packaging, labelling, inventory control, cold chain storage, and distribution of clinical trial supplies in compliance with GCP, GDP, and GMP standards. The candidate will coordinate with various stakeholders to ensure timely and compliant supply chain operations for clinical trials.

Responsibilities include:

• Managing clinical demand and coordinating with manufacturing and clinical teams to ensure supply needs are met.
• Establishing and maintaining documentation and SOPs related to clinical supply chain activities.
• Overseeing inventory, shipments, and site destruction/returns strategies.
• Ensuring regulatory compliance and proper documentation in TMF and other records.
• Collaborating with external partners and internal teams to optimize supply chain processes.
• Monitoring budgets, risk assessments, and quality issues related to clinical supplies.

Qualifications:

• Experience in pharmaceutical supply chain management, especially with clinical trials across multiple territories and sites.
• Knowledge of GXP, GCP, GMP, and related documentation.
• Experience with ERP systems and label design for multi-language countries.
• Strong stakeholder management and communication skills.

We offer:

• Hybrid working environment with flexibility.
• Competitive benefits including pension, life insurance, annual leave, and performance bonus.

Note: This job posting is active and not expired.