Clinical Trails Monitor II (Remote)

About the role

The role uses clinical trial protocols, visit schedules, enrollment expectations, site activity, shipping constraints, and study risks to determine appropriate start-up quantities and ongoing resupply approaches.

What you'll do

• Identify study characteristics that may affect kit supply, such as enrollment patterns, visit schedules, treatment groups, specialty testing, country restrictions
• Lead discussions with clients and study teams on supply strategy, start-up quantities, resupply approach, service scope, risks, and performance
• Use study data, protocol requirements, and operational experience to challenge requests or assumptions that could increase supply risk, kit waste
• Build alignment across stakeholders by clearly communicating decisions, tradeoffs, responsibilities, and required actions
• Develop study-specific start-up kit strategies based on expected enrollment, screening assumptions, site activation plans, visit timing, country lead times

What you need

• 10–18 yrs of experience
• Supply chain
• Clinical research
• Quality control
• B.Sc

Good to have

• Logistics
• Excel
• Operational risk