Global Clinical Supply Specialist – LATAM & Europe

Worldwide Clinical Trials; Dublin; On-site; EUR 55,000 - 75,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Supply Specialist to plan, implement and monitor the study supply strategy within our global CRO. You will collaborate with Project Management, Vendor Management and DLS Leadership to optimise efficiency and ensure quality across the supply chain.

The role requires a Bachelor's in Life Science or related field, 1+ year in clinical research and supply chain operations, and hands-on IRT experience preferred.

Qualifications

• Bachelor's degree in Life Science or a related field.
• Clinical research experience required (1 year minimum).
• Clinical supply chain operations experience required (1 year minimum).
• Hands-on experience with supply chain functionality in an IRT system (preferred).

Responsibilities

• Plan, implement and monitor study supply strategy and overall supply chain to maximize efficiency.
• Optimize supply levels to ensure continuity while minimizing carrying costs; control processes.
• Collaborate with Project Management, Vendor Management, and DLS Leadership.
• Develop and maintain detailed inventories of study drug.
• Develop procedures to increase efficiency while ensuring quality and safety; implement changes.
• Collaborate with DLS Leadership to define and implement KPIs at study and functional levels.
• Identify process bottlenecks and implement solutions in a timely manner.
• Performs other related duties as assigned.

Skills

Planning

Structured thinking

Time management

Problem solving

Relationship management

Negotiation

IT literacy

Risk management

Education

Bachelor's degree in Life Science or related field

Tools

IRT system

Excel

Job description

Worldwide Clinical Trials is seeking a Clinical Supply Specialist to plan, implement and monitor the study supply strategy within our global CRO. You will collaborate with Project Management, Vendor Management and DLS Leadership to optimise efficiency and ensure quality across the supply chain.

The role requires a Bachelor's in Life Science or related field, 1+ year in clinical research and supply chain operations, and hands-on IRT experience preferred.