A Job? Or a Lifetime Experience? Start Yours Here! We are a Portuguese technology consulting company with a strong outward look to the rest of Europe. We have 12 years of experience in the market and
The Mid-Level Pharmacovigilance Analyst will manage the preparation and submission of RPBR/PBRER and PGR/RMP reports, ensuring compliance with regulatory requirements and supporting process improvements. Key Responsibilities Prepare and review RPBR/PBRER and PGR/RMP reports independently. Coordinate with
The Senior Pharmacovigilance Analyst will lead the preparation, review, and submission of RPBR/PBRER and PGR/RMP reports, ensuring compliance with global regulations and mentoring junior staff. Key Responsibilities Lead the preparation and submission of RPBR/PBRER and PGR/RMP reports.