Join Covance and our FSPx Department!
We are actively recruiting a Clinical Study Unit Safety Assistant to join the team of one of our client based in Brussels.
As part of this role, you will be involved in Pharmacovigilance and Safety tasks related to clinical studies and programs in humans.
This is an exciting opportunity to grow in a dynamic and motivating environment where team work is valued.
Provide assistance to the Clinical Study Unit Safety Lead in defined Pharmacovigilance tasks and safety documentation
Reporting of safety events according to Local Regulations and Corporate and Local Quality Documents
Ensure that minimum criteria for received cases are completed, supporting documents
translated into English (if applicable), and forwarded to GPV, in a timely manner
Review AE and contact CRA (if available / necessary)
Send case information to GPV
Reception of acknowledgement of receipt
SUSAR Management for BE / NL / UK / Lux / Ireland
SASR / DSUR Management for BE / NL / UK / Lux / Ireland
When joining Covance you will be :
Welcome in a supportive team environment
Receive on-the-job training and mentoring if needed or be a mentor to others
Enjoy the benefits of working for a company that values a WORK / LIFE BALANCE
Education / Qualifications
Professional bachelor or equal by experience
Fluency in French, Dutch and English
Professional experience : professional experience in Drug Safety,
Clinical Development or Clinical Research is an advantage
Experience working in clinical studies (eg. Previous CPA, CRA experience or similar)
Professional experience in Drug Safety Development or Clinical Research is an advantage
If you are interested in knowing more about Covance and this thrilling opportunity, contact Recruiter Christelle.segabiot covance.com.