1 - 10 van 21 vacatures voor Site Administrator

For one of our customers, global IT market leader we are looking for a permanent TeamSite consultant. Candidates should be fluent in English. Responsabilities: General administration, Incident, Change and Release management. Communication ...

For one of our customers, global IT market leader we are looking for a permanent WebSphere Application Server Portal expert in Brussels. Candidates should be fluent in English. Responsabilities: General administration. Incident management ...

: General administration. Incident management. Change and Release management. Communication with other support teams (webserver teams, unix/linux teams, peoplesoft competence centre…) Coordinate releases between on site and offshore. Coordinate ...

The main responsibility of the Data Management Assistant (DMA) is to assist the data management department with all trial related administrative work.• Support the CDM (Clinical Data Manager) and data management trial teams• CRF ...

the business in the Benelux.They are today recruiting 2 Sales Administrators who will be in charge of the following tasks and responsibilities:-encoding purchase orders using AS 400-handling incoming phone calls-liaising with clients, answering their questions ...

phone calls, emails and correspondence•Welcoming visitors•Ordering office supplies•Liaising with suppliers and service providers•Providing administrative support to Partners•Preparing letters and other documents•And so much more! EXCEL CAREERS is a ...

About SASSAS is the leader in business & analytics intelligence (software and services), and the largest independent vendor in the business intelligence market. SAS helps customers at more than 45 000 sites improve performance and deliver value ...

As a Clinical Research Associate at PAREXEL, you have the opportunity to be a true clinician. You are able to have the greatest impact on drug and medical device clinical trials by working on-site with the clients and focusing on the clinical trial ...

You take responsibility for the administration and monitoring of clinical research projects according to our Standard Operating Procedures, the ICH-GCP Guidelines and ISO 14155. You analyze and evaluate clinical data, ensure compliance ...

department (team of 8 people).Your responsibilities will include:- diary management and organising meetings- interfacing with suppliers, reviewing contracts- managing and administrating expenses using in-house database- preparing documents, letters ...