Senior CRA Oncology Belgium

Diegem, Machelen
negociable
31 Jul 2019
30 Aug 2019
IH-19003546
Full Time
Permanent
Experienced (non-manager)

We are currently looking to strengthen our Clinical Monitoring team in Belgium and are seeking a Senior CRA for our Oncology Business Unit to be based in our brand new Diegem office. We do offer flexible working hours, so than you can plan your day as efficient as possible. Working from home is also a possibility. 

In this role you will be involved in:

  • Site management and site staff performance including monitoring all types of clinical trials ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
  • Data Handling, Reporting and Tracking & administrative tasks
  • You would also perform management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines

We are looking for an enthusiastic and positive colleague with previous experience in monitoring oncology trials. At this moment the focus would be on breast trials, so experience in that area would be an asset. It is necessary that you would be able to monitor both in Dutch and French.

If you would be interested to find out more, please contact one of our recruiters Irene Houtsma or Eveline Wigtman and we are more than happy to speak with you over a cup of coffee!

 

About us: 

Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 23,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.

We understand that cancer is not one disease, but a category of widely varying diseases, each with its own specialized scientific complexities, patient populations and range of treatment options. Our Oncology and Hematology practice is dedicated to the execution of clinical trials in these complex indications and is staffed by dedicated professionals with backgrounds in oncology drug development in academia, industry and CRO settings. This expertise, combined with our Trusted Process® methodology for delivering dependable trial outcomes, provides the resources, clinical expertise and development know-how to help our clients with every facet of their Oncology research