Clinical Supply Associate
Core
Support Clinical Supply Chain Management in delivering clinical material and associated information to meet agreed clinical demand for innovative medicines.
Role type
Clinical Supply Associate (CSA)
Builds
Clinical material and associated information for global clinical trials
Domain
Life Sciences / Bio-pharmaceuticals
Deliverable
client delivery
Required skills
Documentation and coordination, Product Quality Complaints management, Deviations management, Electronic Trial Master File management, Inspection readiness facilitation, User Acceptance Testing, Supply Chain Management systems utilization, Process improvement
Preferred skills
Leadership skills, Enterprise acumen, Visual management, Problem solving, Global standardisation
Technologies
Electronic Trial Master File, Supply Chain Management systems
Responsibilities
Documentation and coordination of Product Quality Complaints; Coordination of Product Quality Sample Returns; Documentation and facilitation of Deviations affecting product quality or regulatory compliance; Management of documents in the electronic Trial Master File; Facilitation of documentation activities ensuring inspection readiness; Utilising Supply Chain Management systems to support agile ways of working; Continually improving the Clinical Supply Chain processes
Seniority
Individual Contributor
