Regulatory RIMS Specialist
- France
- Contract
- Drug Safety / Pharmacovigilance
This is a unique opportunity for a Regulatory RIMS Specialist to join our client – an esteemed partner for regulatory and compliance in healthcare. This is a contract opportunity of at least 6 months within the stunning city of Paris/London. With a globally established presence spanning over 140 countries and partner to some of the top pharmaceutical companies, this is a fantastic company to join to progress your career.
Responsibilities
- Supporting Regulatory Affairs Officers in their routine use of Veeva RIM
- Carry out activities with them in RIM, or for them in RIM
- Suggest improvements in use, on a specific case or on processes in general
Requirements
- Experience as a Regulatory Affairs Officer
- Good knowledge of regulatory processes and issues as a whole
- Advanced contribution to projects, project management
- Animation of community / communication
If this role is of interest to you, please apply now!
#LI-KT1
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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Kathryn
I manage this role.