Quality Specialist - II (Associate)

Quality Specialist - II (Associate) Jersey City, NJ- 100% remote role. 3 Months extendable contract Pay : $45.86/hr Under the direction and oversight of the PV Quality and Compliance Associate Director, this role will: • Perform reviews of individual case safety report compliance monitoring outputs to ensure high quality and compliant reporting in accordance with PV regulations and business partner agreements. • Assist with the development and implementation of processes used to monitor the compliance of individual case safety reports • Participate in compliance monitoring special projects as needed to ensure data quality . Quals. Education and Experience: • Bachelor's degree/Master's degree in life science with minimum 4-5 years of relevant experience within investigation, deviation in the Pharmacovigilance( PV) space. • Strong analytical skills and quality focus • Knowledge of Pharmacovigilance principles, systems, and requirements in addition to Pharmacovigilance regulations • Experience with Pharmacovigilance investigations or deviation management Software expertise: • Office 365 applications • Safety database(ARGUS is preferable) • Will consider someone with similar software experience to ARGUS. Note: • 3 months assignment with possibility of extension. • 100% remote role. • Should have there own laptop or desktop to perform the work.

Created: 2024-10-29