RA/PV Specialist

Our client who specialises in the pharmaceutical industry is looking for a RA/PV Specialist. Your roles and responsibilities will include: 

• Preparing, submitting, tracking, and archiving technical documentation, amendments, reports, and correspondence related to EU filing submissions. 
• Ensuring timely submissions to competent authorities and maintaining organized records
• Prepare and submit regulatory documents for EU filings
• Track the status of submissions and maintain an organized archive of technical documents and correspondence
• Collaborate with regulatory teams to ensure timely and accurate submissions to EU authorities

• Strong written and verbal communication skills, with the ability to convey complex technical and scientific information clearly
• Team-oriented with excellent collaboration abilities
• Science Degree or similar

• 3 to 5 years of proven experience in Regulatory Affairs or Pharmacovigilance

• Health Insurance