My client, a global pharmaceutical company, is seeking a Triage Manager to join their Drug Safety and Pharmacovigilance Department. This Triage Manager will be responsible for collecting and processing adverse events that have been entered into their global central safety database, Argus 7.
The client is based in Danbury, CT and will require 5 days/wk of on site working forat least the first 3 months. After the first 3 months if the performance is strong, they will gradually add in remote working for up to 3 days/wk; however, it will never a fully remote position.
I have included details below; if you're interested, please send an updated resume and Victoria from Real Staffing will be in touch!
Job Title: Triage Manager
Hours Per Week: 40.00
Location: Danbury, CT - can do some remote working after 3 months
Duties: Directly responsible for ensuring that adverse events are processed, analyzed and reported according to Corporate SOPs, local working instructions and local regulatory requirements. Responsible for distribution and retrieval of data to internal and external customers as needed for analysis and compliance with regulations. Serve as point of contact with clinical team in areas of adverse events process. Assist with collection, processing, and reporting on adverse event reports.
Skills: Pharmaceutical Industry experience. Must possess solid understanding of federal regulations as they apply to drug surveillance for both IND and NDA reporting. Strong communication skills required in order to facilitate report preparation, participate in working groups and interact with a variety of departments. Experience with computerized data entry and retrieval as well as other computer based applications (word/excel) is also required
Education: Bachelors Degree in biomedical science or equivalent and a basic knowledge of clinical medicine