Associate/Senior Associate - ETS-Registration Tracking Lead Administrator

Kalamazoo, Michigan

Posted in Pharmaceuticals

This job has expired.

Job Info

Role Description

This position requires a basic understanding of pharmacovigilance (PV) practices with the responsibilities of applying this knowledge to assure regulatory compliance. This position contributes to regulatory activities focused on maintaining the product dictionary for company products. This position requires the ability to organize and compile the required information and documents for maintenance of the products in the product dictionary which interacts with other company databases. This role serves as the ETS-Registration Tracking Lead Administrator (Admin) and collaborates with other ETS-RT global Admins. This position may contribute to special project work as assigned. This position requires strong interpersonal, communication, database management and time management skills.

Responsibilities include but are not limited to:
- Facilitates the activities of the ETS-RT Admin team, including leading meetings, recording meeting minutes, and executing action items that the Admin Team has aligned and agreed to.

- Liaises with the Business Support Team to assure timely updates and execution of data elements in the ETS-RT database.

- Maintains the ETS-RT WIKI page training documents and information.

- Leads data quality improvement initiatives.

- Trains colleagues in using the ETS-RT database (including Business Objects to retrieve data from ETS-RT) as appropriate and approves access to the ETS-RT database.

-Proficiency in using Microsoft Office, including Outlook and Excel.

Basic Qualification:

Degree in biology, animal science, pharmacy, business or other related science.

Optional: Experience in pharmacovigilance adverse event submissions and Business Objects queries is a plus.

Full time



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This job has expired.

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