Job Description:
- Accurate and timely data entry of both domestic and foreign adverse event information into the PSSS (Product Safety Surveillance System) consistent with the ARISg coding manual, SOPs/WIDs, process flows and established time frames within the ARISg workflow.
- Full understanding of the products’ Company Core Data sheet(CCDS), PI, and/or IB for accurate labeling and listedness.
- Ensure accurate and timely submissions to regulators, co-marketing partners and affiliates within company and regulatory timeframes.
- Complete all required training within the timelines provided so as to ensure knowledge of all relevant corporate and departmental SOP’s, SWP’s and WID’s.
- Gather sufficient information to assess the medical significance of an adverse event report.
Requirement:
- Bachelor’s degree in healthcare field.
- Minimum 2 to 4 years in pharmaceutical Drug Safety
- Experience with MedDRA coding/WHO coding.
- Experience with ArisG/Argus.
- Medical terminology and standards of patient care
- Computer proficiency
Job Type: Contract
Salary: $30.00 - $35.00 per hour
Schedule:
- 8 hour shift
- Monday to Friday
Education:
- Bachelor's (Required)
Experience:
- ARISg: 4 years (Required)
- Drug Safety: 4 years (Required)
Work Location: Remote