Lead, Trial Delivery Management
Pubblicato il 14-09-2026 - Johnson & Johnson in Milano
Overview
In this Lead, Trial Delivery Management role, you drive end-to-end trial delivery across multiple countries, coordinating feasibility, risk reviews, vendor management, and trial-level operations. You will align regional delivery with program goals, mentor teammates, and support inspections, shaping how trials translate into clinical impact. This position sits at the intersection of R&D operations and Innovative Medicine, offering global scope and meaningful patient outcomes. You will work with cross-functional teams to optimize study execution and risk mitigation.
Retribuzione / Benefits
- annual premio with target pay based on location
- vacation days
- parental leave (min 12 weeks)
- bereavement leave
- caregiver leave
- well-being reimbursement
Responsabilità
- Create and update critical trial documents (e.g., monitoring guidelines, ICF, IMP-related docs).
- Manage setup and ongoing oversight of trial vendors, including SOWs and budgets.
- Coordinate country/regional trial activities and align feasibility strategies with local teams.
- Contribute to program-level compound training with Clinical/CTL&D;/Medical Writing.
- Input into trial-level operational strategies and mitigation of trial risks.
- Participate in process improvements at trial, compound, and cross-DU levels.
- Support Health Authority inspections and risk mitigation planning at the program level.
- Mentor and onboard new Trial Management team members.
Requisiti fondamentali
- BS degree or equivalent; Life Sciences fields preferred.
- Minimum 4 years of clinical trial experience in pharma/healthcare or related industries.
- Experience across multiple trial phases (I-IV) and ability to manage multiple aspects of trial execution.
- 2-3 years’ experience supporting global clinical trials.
- Strong leadership and ability to work in multi-functional, matrixed, global environments.
- Excellent decision-making, analytical, and financial management skills.
- Ability to operate with limited supervision and mentor others.
- Strong project planning, communication, and presentation skills.
- Travel up to 15–20% as needed.
- leadership
- communication
- problem solving
- Clinical Trial Management Systems (CTMS)
- Regulatory Compliance
- QA and SOP adherence