CRA (open for international travel)

For one of our clients located in the east side of Brussels, we are looking for an experienced Clinical Research Associate.

  • Do you have a Master Degree in Life Sciences?
  • Do you have a first experience as a CRA or as a Study Coordinator?
  • Are you fluent in English?

Then, you might be the candidate we are looking for!

Job Description 

As a CRA, you are responsible for “on-site” quality control of clinical trials to ensure that a clinical trial is conducted, recorded and reported in accordance with the protocol, the principles of Good Clinical Practice (GCP) and the applicable regulatory requirements.

Responsibilities 
  • You perform on-site monitoring visits according to the monitoring plan and following the company's Standard Operating Procedures (SOPs) and ICH-GCP guidelines
  • You ensure and control sites’ compliance with the study protocol and regulatory obligations
  • You address issues in a manner that is beneficial for the site and the team
  • You report the findings of the “on-site” monitoring visits according to the company's Standards
  • You follow the sites’ findings until resolution, with the support of the study team and Quality Assurance and Control unit
  • You perform site staff training whenever needed during the study conduct
  • You ensure close collaboration between all actors of clinical trial research, as a privileged link between investigational sites and the study team
Profile 
  • You have a University degree in Life Sciences
  • You have practical knowledge of the conduct of clinical trials
  • You have the first experience as a CRA or as a Study Coordinator
  • You  have previous experience in Oncology
  • You are open to travel 40% of the working time across European countries
  • You are fluent in English (written & spoken) and you speak at least one other EU language (French, Dutch, German, Italian, Spanish)
  • You have excellent organization skills
  • You have good communication skills
  • You are proactive and dynamic
  • You are independent and team-player
Contact Information 

Ariane d'Ansembourg
+32 10 68 53 30
ariane.dansembourg@valesta.com

Application form : CRA (open for international travel)

Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.

I want to stay informed.

I would like to receive Valesta news, valuable insights into industry trends, career opportunities, trainings, and other helpful tips to find assignments that match my skills and interests. Click here to stay connected with Valesta.

Valesta is an expert in life science recruiting and project staffing.  The information you are submitting is important for us to respond to your assignment and contract needs. In compliance with the General Data Protection Regulation (EU) 2016/679) (“GDPR”), Valesta will process your personal data in accordance with our Privacy Policy. Valesta will safeguard your personal information and not disclose to any person unlawfully. As a staffing company, Valesta receives and processes your personal data for the following purpose: to take appropriate steps to find you an assignment with one of our clients and/or to finalise a contract with you.

Please note that Valesta does not wish to receive any data from you if you are under the age of eighteen (18) or data that is classified as Sensitive Data under the GDPR; this includes personal data revealing racial or ethnic origin, political opinions, religious or philosophical beliefs, trade union membership, genetic/biometric/health-related data or data concerning a person's sex life/sexual orientation.

Please read our disclaimer.