Global Trial Delivery Lead

Leiden Bio Science Park; Leiden; On-site; EUR 90,000 - 140,000; Full time

Job summary

Leiden Bio Science Park is seeking a Lead, Trial Delivery Management to oversee study-level execution, document control, and vendor oversight across country/regional delivery. You will align feasibility, set targets, perform risk reviews, and address local challenges impacting study delivery.

The role requires 4+ years in clinical trials, strong leadership, and collaboration across global teams. Travel up to 15–20% is expected, with opportunities to mentor new staff and support inspections.

Qualifications

• BS degree or equivalent in Life Sciences.
• Minimum 4 years clinical trial experience in pharma/healthcare.
• Experience across multiple study phases (I–IV).
• 2–3 years supporting global clinical trials.
• Strong leadership and mentoring abilities.
• Ability to work with limited supervision.
• Travel 15–20% as required.

Responsibilities

• Create and update critical trial-specific documents (e.g., Monitoring Guidelines, ICF, IMP-related documentation).
• Manage vendor setup and day-to-day vendor activities including SOW creation and budget oversight.
• Coordinate country/regional trial management activities and oversight with local teams.
• Support development of program-level compound training with Clinical / CTL&D / Medical writing.
• Provide input into trial level operational strategies and risk reviews.
• Resolve trial-related issues and mitigate risks; participate in process improvements.
• Mentor onboarding of new team members and support inspections when needed.

Skills

Leadership

Project management

Communication

Risk management

Vendor management

Cross-functional collaboration

Mentoring

Analytical thinking

Strategic planning

Budget oversight

Education

Bachelor's degree in Life Sciences

Tools

CTMS

Job description

Leiden Bio Science Park is seeking a Lead, Trial Delivery Management to oversee study-level execution, document control, and vendor oversight across country/regional delivery. You will align feasibility, set targets, perform risk reviews, and address local challenges impacting study delivery.

The role requires 4+ years in clinical trials, strong leadership, and collaboration across global teams. Travel up to 15–20% is expected, with opportunities to mentor new staff and support inspections.