Carriere Switch

Deze vacature is ouder dan 40 dagen...

6

sollicitanten

Reddingsgeld om snel wat extra geld te bekomen in tijden van nood. Lenen t/m Euro 300,- met een looptijd van 10 tot 28 dagen.


Decat, Denewet & Van Berckelaer (Dedevan), founded in 2006, is the preferred partner (national as well as international) in healthcare outsourcing for clinical research in the pharmaceutical, medical devices and biotechnology industry. We are successful in recruiting, training and providing experienced people. Thanks to Dedevan’s unique healthcare outsourcing’s concept, we respond to the increasing need for clinical research professionals.

We are looking to hire a Drug Supply Coordinator (VAC/170)


Company:
A leading pharmaceutical company.


Job description:

The Drug Supply Coordinator defines and implements the optimized strategy of packaging and shipment of Clinical Trial Supplies for (Immunotherapeutics) studies.

Core responsibilities:
• Ensure delivery of adequate clinical supplies within defined timelines at any time during trial duration;
• Forecasting of drug product, comparators and of packaging workload;
• Review protocols, analyze and evaluate feasibility and consequences of proposed designs & ensure on time development of Pharmacy manual;
• Translation of the protocol into packaging and labelling requirements, bearing in mind all technical aspects and local regulations;
• Create, approve & follow up the supply request in the official system;
• Coordinate the return and destruction of supplies whenever needed;
• Participation to monitor meetings, present all logistical aspects of a study, organize workshop sessions as appropriate;
• Give training on cold chain and logistics whenever necessary;
• Reference person for all drug supply related issues within the Clinical Project Team;
• Coach and supervise a Drug Supply assistant/coordinator;
• Manage filing of all study related information.


Profile:

• Master degree in Sciences or equivalent background;
• At least 2 years experience in a clinical trials environment, monitoring experience is an asset;
• Good knowledge of ICH-GCP and understanding of Global Study Management roles and activities;
• Understanding of regional organization and of Local Operating Countries structure;
• Excellent communication skills in English, good knowledge of French and Dutch;
• Computer literate.