Lead, Trial Delivery Manager - 2 Positions

Johnson Johnson; Bardi; In loco; EUR 90.000 - 130.000; Tempo pieno

Vantaggi offerti da questo lavoro

Extensive benefits package

Flexible working environment

Parliamentary/ parental leave options

Descrizione del lavoro

Johnson Johnson in Italy seeks a Lead Trial Delivery Manager to oversee study-level execution and vendor oversight across countries, ensuring trial plans align with local capabilities.

You will shape operational strategies, manage risk, mentor Trial Management staff, support Health Authority inspections, and contribute to patient-focused medicines from lab to life.

Competenze

• BS degree or equivalent; 4+ years clinical trial experience in pharma/healthcare.
• Experience across multiple study phases (I–IV).
• 2–3 years supporting global clinical trials.

Mansioni

• Create and maintain critical trial documents (e.g., Monitoring Guidelines, ICF, IMP-related docs).
• Manage vendor setup, on-going vendor activities, SOW creation and budget oversight.
• Coordinate country/regional trial management activities and risk reviews.
• Contribute to program-level compound training with Clinical/CTL&D/Medical Writing.
• Provide input on trial-level operational strategies and resolve trial-related issues.
• Participate in process improvement at trial/compound/cross-DU levels.
• Support Health Authority inspections and risk mitigation planning.
• Mentor onboarding and development of Trial Management staff.

Conoscenze

Leadership

Communication

CTMS

Regulatory Compliance

SOPs

Financial Management

Mentoring

Formazione

BS degree or equivalent

Strumenti

CTMS

Descrizione del lavoro

As Lead Trial Delivery Manager, you drive study-level execution and vendor oversight across countries, ensuring trial plans align with local capabilities. You will shape operational strategies, manage risk, and mentor team members to deliver high-quality clinical research. This role sits at the intersection of trial management and cross-functional delivery within a mission-driven, innovative healthcare environment. You will help scale studies and support inspections, contributing to patient-focused medicines from lab to life.

• extensive benefits package
• flexible working environment
• vacation days—parliamentary leave/parental leave options
• Create and maintain critical trial documents (e.g., Monitoring Guidelines, ICF, IMP-related docs)
• Manage vendor setup, on-going vendor activities, SOW creation and budget oversight
• Coordinate country/regional trial management activities and risk reviews
• Contribute to program-level compound training with Clinical/CTL&D/Medical Writing
• Provide input on trial-level operational strategies and resolve trial-related issues
• Participate in process improvement at trial/compound/cross-DU levels
• Support Health Authority inspections and risk mitigation planning
• Mentor onboarding and development of Trial Management staff
• BS degree or equivalent; 4+ years clinical trial experience in pharma/healthcare
• Experience across multiple study phases (I–IV) and management of multiple trial aspects
• 2–3 years supporting global clinical trials
• Strong leadership; ability to work in matrixed global environments
• Excellent decision-making, analytics, and financial management skills
• Ability to operate with limited supervision and mentor others
• Experience hiring, training, and evaluating staff
• Strong project planning, communication, and presentation skills
• leadership
• communication
• Clinical Trial Management Systems (CTMS)
• Regulatory Compliance
• SOPs

Lead, Trial Delivery Manager - 2 positions pavia, lombardia, it