Drug Safety & Adverse Event Specialist

Biotech Networks, LLC; Plainfield (NJ); On-site; USD 60,000 - 90,000; Full time

Job summary

Biotech Networks, LLC is seeking a candidate for the Quality & Regulatory Compliance (Clinical Operations) team in New Jersey. The role centers on processing and reporting adverse events and overseeing safety data for marketed and investigational products.

The position involves coordinating with clients and internal teams to ensure accurate data entry into the Product Safety database and compliance with regulatory requirements.

Responsibilities

• Processing & reporting Adverse events into the Product Safety database for in association with Client’s Marketed and investigational products.
• Perform processing and oversight of adverse event/drug experience reports (serious and non-serious) and other safety related data for marketed products and clinical studies.

Job description

Biotech Networks, LLC is seeking a candidate for the Quality & Regulatory Compliance (Clinical Operations) team in New Jersey. The role centers on processing and reporting adverse events and overseeing safety data for marketed and investigational products.

The position involves coordinating with clients and internal teams to ensure accurate data entry into the Product Safety database and compliance with regulatory requirements.