Clinical supply chain

General duties and responsibilities:

·      manage distribution from warehouses to clinical sites

·      Manages and maintains collaboration with clinical study team in order to define study timelines, kit design and supply planning.

·      Oversee study packaging, labeling and storage activities for clinical trials

·      Participates in the review of study protocol, collects and communicates suggestions for a protocol change to responsible author.

·      set-up and maintenance of IVRS / IRT system In collaboration with Clinical Operations and CRO.

·      Monitor regularly drug expiry, and the appropriate inventory re-supply

·      Responsible for Accountability, Returns and Destruction of supplies

·      Ensures compliance of the clinical supply activities with the ICH GCP, GMP, GDP guidelines and SOPs.

·      Initiate efforts for improving current processes for better efficiency and faster turn-around.

%2A     And any other task assigned by direct manager

 

Competencies:

·      Expirience in clinical supply chain

·      Strong communication and organisational skills

·      Ability to flag issues in a tiemly manner and perform issue escalation

·      Flexible and able to work in a global changing enviroment, multi tasking and deadllines

·      Teamplayer who can also operate independently

·      Solution-oriented and problem solving attitude

·      Service oriented

Education and Knowledge Requirements:

·      College degree or higher, preferentially in pharmacy/ engineering /sciences/supply chain

·      At least 3 years of experience in a pharmaceutical industry or supply chain or project  mangement

·      Computer literate

·      Fluent in English – Must

Travel %28up to 20%%29 may be required, including international travel