Specialist, Regulatory Affairs

To ensure that the clients are fully supported in all regulatory submissions with assistance from the manager or other senior team member. To function with a degree of independence and is responsible for creating eSubmission compliant documents and submissions, troubleshooting, with help from the manager as required.

• To ensure that the clients are fully supported in all regulatory submissions with assistance from the manager or other senior team member.
• To function with a degree of independence and is responsible for creating eSubmission compliant documents and submissions, troubleshooting, with help from the manager as required.

• High-level understanding of regulatory processes and CTD dossier structure - Modules 1 to 5.
• Prior experience with eDMs, RIM tools or eCTD publishing software like docuBridge, eCTD manager, Veeva or other, is not required but is an advantage.

• Total rewards
• Career areas
• Equal Employment Opportunity

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere.