CRA België - single sponsor

Posted on Mar 16, 2019 by Syneos Health

Not Specified Belgium
Research & Development
14 Mar 2019
Annual Salary
Full-Time
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. Evolve in a global company that is always looking for ways to work smarter and more efficiently as the only fully integrated Biopharmaceutical Accelerator. You'll be supported with comprehensive resources based on today's emerging technologies, data, science and knowledge - instead of practices from the past. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment to over-deliver and outperform.
A career with Syneos Health means your everyday work improves patients' lives around the world.

We are currently looking to strengthen our Clinical Monitoring team in Belgium seeking a Clinical Research Associate for one of our business units solely focused on one single sponsor. In this role you can be home-based, but you are also more than welcome to work from our brand new office in Diegem.

A brief summary of duties you will be involved in:

Monitoring all types of clinical trials and participating in all types of site visits ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
Data Handling, Reporting, Tracking and administrative tasks
Performing management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines.

To succeed in this role you will need the following skills/experience:

Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position
Previous nominal practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO in CNS area
Basic understanding of SOPs, WIs, FDA, and local regulations as well as ICH GCP guidelines
Good command of written and spoken English, French and Dutch language

If your application is successful you will be contacted by one of our dedicated Benelux recruiters, Eveline Wigtman and Irene Houtsma. They will be more than happy to meet you!

Reference: 671584490