*summary*:
the clinical supply manager provides support for strategic planning, forecasting, and managing activities related to the procuring, packaging and distribution of clinical supplies that support sponsored, investigator initiated, expanded access and research collaboration trials. They will participate in cross-functional teams which include our internal operations, approved third-party vendors and global supply partners.
*about the role*:
*key responsibilities*:
- forecasting: maintain accurate demand forecasts to ensure availability of clinical supplies while minimizing excess inventory and reducing waste.
- procurement: oversee the ordering of investigational medicinal products (imp) and commercial drugs, ensuring timely and cost-effective delivery of high-quality materials. Facilitate import requirements by coordinating logistics documents.
- inventory management: monitor and maintain inventory levels to ensure adequate supply for ongoing and upcoming clinical trials.
- budget management & forecasting: maintain budget forecasts to ensure accurate financial planning and control of clinical supply chain expenses. including purchase orders (po), and invoice approval.
- vendor management: establish and maintain relationships with approved third-party vendors and global supply partners, ensuring they meet performance standards and contractual obligations.
- cross-functional collaboration: work closely with internal teams, including operations, quality assurance, and clinical operations, to ensure seamless coordination of supply chain activities.
- compliance: ensure all supply chain activities comply with relevant regulations, guidelines, and company policies.
- problem-solving: address and resolve supply chain issues and challenges promptly and effectively.
- reporting: prepare and present regular reports on supply chain performance, including key metrics and improvement initiatives.
- drives and manages kpi: drive and manage key performance indicators (kpi) to ensure optimal supply chain performance..
*essential requirements*:
- advanced english, level c1 - c2
- bachelor's degree in supply chain management, business administration, life sciences, or a related field.
- strong knowledge of supply chain management principles and best practices.
- excellent project management and organizational skills.
- proficient in data analysis and demand forecasting techniques.
- familiarity with regulatory requirements related to clinical supply chains.
- effective communication and interpersonal skills.
- ability to work collaboratively in cross-functional teams.
- detail-oriented with strong problem-solving abilities.
- technical proficiency: competency in supply chain management software and microsoft office suite.
- proven ability to work independently and ability to collaborate and work effectively in teams. Demonstrated ability to support multiple projects.
*commitment to inclusion*
novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Division
operations
business unit
universal hierarchy node
location
mexico
site
insurgentes
company / legal entity
mx06 (fcrs = mx006) novartis farmacéutica s.a. de c.v.
Functional area
research & development
job type
full time
employment type
regular
shift work
no
*accessibility and accommodation*:
novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.