Senior Regulatory Operations Associate

We are seeking a Senior Regulatory Operations Associate to join our team. As a Senior Regulatory Operations Associate, you will play a pivotal role in managing regulatory documents and processes, contributing to the successful execution of clinical trials and the advancement of innovative treatments and therapies.

Requirements

• Bachelor's degree in a scientific or related field
• Minimum of 3 years of experience in regulatory publishing within the pharmaceutical, biotech or CRO industry
• Proficiency in electronic document management systems (eTMF, eCTD) and regulatory submission software
• Canadian submission background is preferred but not required
• Strong understanding of regulatory requirements and guidelines for clinical trials
• Excellent organizational, communication, and problem-solving skills

Benefits

• Various annual leave entitlements
• A range of health insurance offerings
• Competitive retirement planning offerings
• Global Employee Assistance Programme
• Life assurance
• Flexible country-specific optional benefits