Clinical Research Associate

As a CRA, you oversee the progress of a clinical trial on national level, ensuring that it is conducted, recorded and reported in accordance with the protocol, applicable Operating Procedures (SOPs), the highest quality standards defined by Good Clinical Practices (GCP) and the relevant local regulations.

Intense interaction and communication with doctors and nurses, logistic support to the medical team, quality control on data and processes with a primary focus on patient safety, are your daily tasks.

You will work across a range of studies and therapy areas. You will be responsible for site management from selection over start up and recruitment till study closure. You will ensure that recruitment targets are met by building strong relationships with site staff whilst ensuring that the trial is run to the standards requirements.

Profile:

You should have a Master degree (or equivalent) in a scientific or medical discipline; previous experience in clinical research is not required but will be a definite asset; be ready to travel at a national level (up to 70% of your time).

Competencies:

Successful candidate should be able to communicate efficiently on different levels, be assertive and can work on several projects at once with high flexibility, be detail oriented and have excellent time management and organizational skills.
In addition you need to have a driving license and be tri-lingual Dutch – French - English.

What we have to offer:

Quintiles offers attracting salary & benefit packages that will be discussed individually.