Clinical Distribution Associate
Clinical Distribution Associate – Documentation or administrative Tasks, GMP/GCP, clinical supply chain
Role:
For our client in the Pharma industry based in Kaiseraugst we are looking for a Clinical Distribution Associate.
Global Clinical Distribution (PTDS-L) is responsible for the worldwide distribution of clinical trial materials for open and blinded clinical studies. Our Global Clinical Distribution Leads (GCDLs) operate a network of 24 depots around the globe, ensuring delivery of Investigational Medicinal Products (IMPs) and Other Study Drugs (OSDs) to the clinical sites on time, in the right quality and quantity. With our strong distribution team capabilities and complimented by our strategic internal and external depot partners we are able to ensure patient delivery into more than 90 countries. Clinical Distribution (PTDS-L) is responsible for the worldwide distribution of clinical trial materials for open and blinded clinical studies. Our Global Clinical Distribution Leads (GCDLs) operate a network of 24 depots around the globe, ensuring delivery of Investigational Medicinal Products (IMPs) and Other Study Drugs (OSDs) to the clinical sites on time, in the right quality and quantity. With our strong distribution team capabilities and complimented by our strategic internal and external depot partners we are able to ensure patient delivery into more than 90 countries.
Areas of responsibility:
* Processing and surveillance of study specific shipment orders of Investigational Medication Products
* Ensure compliant and efficient execution of the order, distribution and logistics processes on time and in a compliant way
* Issue and prepare timely transfer of products, documents and information
* Maintain and control adherence to trade, customs and tax related compliance standards and provide support for trade or customs related issues in daily business operations
* Preparation of the relevant documents for Import and Export with effective administration for running of order, distribution and logistics operations
* Timely communication to all involved parties
* Act as single point of contact towards different internal and external stakeholder’s e.g. quality,
regulatory or finance/controlling functions for the distribution
* Maintain active communication with 3rd party customers on logistics and distribution operations
* Support and contribute to realization of objectives, projects and improvement initiatives
Professional and technical requirements:
* BSc or MSc in Business Administration, Economics, Supply Chain or Life Sciences with
experience in Documentation
* Min. 5 years’ experience in Logistics Supply Chain, Clinical Supply Chain, Clinical Operations or
the pharmaceutical industry
* Experience in Documentation or administrative Tasks is a MUST
* Experience with GMP/GCP is a plus
* End to end clinical supply chain knowledge is a plus
* Experience in SAP/ G-Suite / MS Office
* Fluency in English is a MUST and German is an advantage
Personal Requirements:
* Customer-oriented mindset and excellent communication skills with different levels
* Outstanding team player with dedication and passion
* Strong planning, organization, time-management and end to end process-thinking skills
* Independent self-starter, negotiate, and build consensus skills
Reference no: 920323 AD
Role: Clinical Distribution Associate
Industry: Pharmaceutical industry
Workload: 100%
Location: Kaiseraugst, Switzerland Home Office: due to Corona after this part-time possible
Start date: asap
Duration: 12 months contract, with possible extension
About us:
ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
