Regulatory Affairs Data Verification Coordinator

At the moment we are looking for a Regulatory Affairs Data Verification Coordinator.

  • Do you have a good understanding of CTD Module 3 data?
  • Do you speak fluent English?
  • Are you flexible and proactive?

Then you are the perfect candidate for this function. So do not hesitate to apply today to find out more.

Job Description 

We are looking for a Regulatory Affairs Data Verification Coordinator to coordinate and support data verification activities in our Marketing Authorisation data tracking system InSight. 

Responsibilities 
  • Coordinate verification of CMC baseline data and MA baseline data in InSight across EMEA Regulatory Affairs teams (Local Operating Companies LOCs and Therapeutic Areas TAs), under the oversight the EMEA RIM InSight Implementation Lead and in close collaboration with the EMEA InSight Data Entry Specialists 
  • Liaise with the global RIM InSight team and CMC RA team on the data verification process, roles and responsibilities, to ensure alignment between global and EMEA expectations
  • Provide GRA EMEA LOCs and TAs with training, guidance and communication on the required verification activities 
  • Support LOCs in verification activities as needed, including performing actual verification where appropriate and possible 
  • Liaise with CMC RA to ensure EMEA verification feedback on CMC data is assessed and actioned 
  • Liaise with EMEA Data Entry Specialists to ensure EMEA verification output is accurately entered/reflected in InSight. 

This role is critical to ensure the accuracy of EMEA data in InSight. The successful candidate should be able to effectively drive decisions and enforce actions in a process which is still developing, take appropriate EMEA decisions independently and escalate when needed. 

Profile 
  • Good understanding of CTD Module 3 data 
  • Understanding of local registration data tracking requirements 
  • Knowledge of compliance requirements and advanced process thinking 
  • Good technical skills 
  • Proven ability to deliver complex projects on time 
  • Ability to work effectively in a matrix organisation with multiple cross-functional stakeholders on global, regional and local level 
  • Excellent cross-cultural communication skills in English 
  • Flexibility and proactivity
Contact Information 

Claire Aerts
+32 15 21 11 04
claire.aerts@valesta.com

 

Application form : Regulatory Affairs Data Verification Coordinator

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.