Strategic Trial Delivery Lead, Clinical Operations

Biopharma Asia; Pennsylvania; Hybride; USD 120 000 - 207 000; Plein temps

Résumé du poste

Johnson & Johnson is seeking a Manager, Trial Delivery Management (TDM) to lead the execution of study-level activities across multiple countries in a hybrid model (Spring House/Titusville/Raritan/Horsham, USA). You will oversee vendor management, regulatory documentation, and program-level training while guiding feasibility alignment and risk mitigation.

The role requires strong leadership, 8+ years in pharma/healthcare, and experience across Phases I–IV.

Qualifications

• BS degree or equivalent; Life Sciences preferred.
• 8+ years in Pharmaceutical/Healthcare or related industries.
• Experience with clinical trial execution across Phases I–IV; manage multi-country studies.
• 2–3 years leading multiple aspects of a global clinical trial.
• Strong leadership, communication, and collaboration in matrixed environments.
• Excellent decision-making, analytical and financial management skills.

Responsabilités

• Create and update trial-level documents (e.g., monitoring guidelines, ICF, IMP documentation).
• Oversee vendors: setup, SOW creation, budget oversight.
• Coordinate country/regional trial management activities and risk reviews.
• Contribute to program-level training and cross-functional collaboration.
• Provide input on operational strategies and risk mitigation.
• Mentor onboarding of new team members and foster Credo behaviors.
• Support Health Authority inspections and issue mitigation planning.

Connaissances

Leadership

Project planning

Strategic thinking

Communication

Mentorship

Financial management

Problem solving

Formation

BS degree or equivalent

Life Sciences or related field

Outils

Clinical Trial Management Systems (CTMS)

Description du poste

Johnson & Johnson is seeking a Manager, Trial Delivery Management (TDM) to lead the execution of study-level activities across multiple countries in a hybrid model (Spring House/Titusville/Raritan/Horsham, USA). You will oversee vendor management, regulatory documentation, and program-level training while guiding feasibility alignment and risk mitigation.

The role requires strong leadership, 8+ years in pharma/healthcare, and experience across Phases I–IV.