As a Manager of Clinical Supplies you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
**What you will be doing**:
- Represent Clinical Supply Chain on Clinical Study Teams and provide a high service level to internal stakeholders.
- Works with Clinical Operations to understand clinical demand requirements and ensures alignment with study teams on clinical supply plans and timelines.
- Develop and maintain clinical supply forecasts (Within forecasting system N-Side) and inventory plans for assigned programs, ensuring alignment with upstream supply integrators.
- Maintain routine and timely communication with Investigational Material Supply Chain (IMSC) Integrators to discuss aggregate drug product demand, changes in clinical supply forecasts, and study timelines.
- Maintain routine and timely communication with Investigational Material Supply Chain (IMSC) Operations to discuss the planning and execution of all packaging and labeling work to support clinical trials.
- Coordinate sourcing of co-meds working closely with Procurement, Supply Vendors and Alliance Managers. Ensure delivery of co-meds to IMSC Operations for further packaging and distribution.
- Generate and monitor co-med budgets and spend working closely with Development Project Managers, Clinical Operations and Finance.
- Manages clinical supply inventory, develops inventory reports and monitors upcoming expiry for assigned programs.
- Align efforts among Project Management, Clinical Operations, and Technical Operations for the timing and delivery of clinical supplies for assigned programs.
- Facilitate discussions and decisions on label and packaging design, as needed.
- Support IRT user acceptance testing, develops IRT supply strategy,



and oversees ongoing supply activities in the system.
- Independently leads cross-functional clinical supply status meetings.
**You are**:
- Bachelor degree in a related field.
- 5+ years of work experience in the pharmaceutical industry.
- 3-5 years of Clinical Supply Chain Management experience is required.
- Knowledge of general clinical trials and the drug development process.
- Knowledge of global pharmaceutical regulatory requirements (e.g. cGMP, GCP).
- Knowledge of IRT system set-up, functionality, and proficiency with excel modeling
- Experience in vendor oversight and managing external partnerships is preferred.
**What ICON can offer you**:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
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📌 Manager of Clinical Supplies (México)
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📍 México