BrightOwl Loader Loading

Head of Pharmacovigilance Unit - Belgium   The Head of Pharmacovigilance contributes to the achievement of the company by providing effective management and academic leadership within her/his unit.

BrightOwl managed [?] Still accepting applications

Project Types : Permanent position ,
FTE : N/A
Min.Experience : Just graduated
Start Date : ASAP
End Date : N/A
Posted on : 10 February 2017

Project is currently here

Step 1
Application
Step 2
BrightOwl Screening
Step 3
BrightOwl Interview
Step 4
Company Screening
Step 5
Company Interview
Step 6
Budgets & Contracts
Step 7
Position filled

Project Description


About us:
  • Our company  promotes cancer research in Europe and is linked to other leading biomedical research organizations around the world.
  • Our research takes place in over 200 hospitals, universities and cancer centers in 32 countries and the unique network of investigators. 
  • Our company comprises more than 2000 clinicians collaborating.
  • Our research facility has a vacancy for a Head of Pharmacovigilance Unit
  • The Head of Pharmacovigilance works under the hierarchical supervision of the Head of Medical, Pharmacovigilance and Fellowship department.

Main responsibilities / Major Activities
  • The Head of Pharmacovigilance contributes to the achievement of the company by providing effective management and academic leadership within her/his unit.
  • The Head of Pharmacovigilance is accountable for matters relating to the management of staff, the organization of the unit and pharmacovigilance activities.
  • The Pharmacovigilance activities include but not limited to: 
    • the processing of individual serious adverse event reports, 
    • preparation of annual safety reports, 
    • implementation and maintenance of the Pharmacovigilance procedures and safety database, 
    • transfer of Pharmacovigilance data, 
    • support to others units, education and trainings.

Other responsibilities
  • Participates in the Eudravigilance Expert Working group. 
  • Represents our company at the MedDRA Usergroup meetings 

Qualifications
  • A scientific university degree in Medicine, Pharmacy, Bioscience or equivalent 
  • 3-5 years in Pharmacovigilance and risk management 

Skills
  • Management skills 
  • Good organization and negotiation skills 
  • Deep sense for responsibility and high degree of self-motivation 
  • Good communication skills with the ability to communicate with diverse individuals and groups. Fluent English (spoken and written) 
  • Knowledge of European PV reporting regulations 
  • Demonstrates computer literacy with proficiency in the used and management of safety databases 

Our Offer:
  • Our company offers a highly stimulating, professional & friendly atmosphere in an international environment, and employees’ benefit. 

Others

Work from home:   Not Allowed
No. of Positions:   1