Job Title: Pharmacovigilance / Drug Safety Specialist (Coordinator) Location: Lawrenceville, NJ – Hybrid Duration:6 Months (Possible extension) Key Responsibilities: • Build and improve data reports and dashboards for pharmacovigilance (PV) and regulatory activities. • Develop and maintain reports in SAP Business Objects, Tableau, or Power BI. • Perform data analysis using SQL or Oracle. • Maintain data integrity across systems and support reporting/visualization needs. • Collaborate with cross-functional teams (e.g., PV, Epidemiology) to deliver actionable insights. • Support validation testing and prepare documentation like test scripts and summary reports. • Participate in innovation and process improvement initiatives. • Create and present reports on team performance, KPIs, and analytical insights. Must-Have Skills: • Advanced SAP Business Objects (report building) • Advanced Tableau or Power BI (interactive dashboard creation) • Advanced SQL/Oracle (data querying & analysis) • Strong MS Office skills (PowerPoint, Excel, Word) Preferred Skills: • Background in Pharmacovigilance or Drug Safety • Knowledge of MedDRA or WHO Drug coding dictionaries • Familiarity with validation processes and documentation • Strategic thinking, stakeholder management, and communication skills Qualifications: • Bachelor's or Master’s in Life Sciences, Information Science, or related field • 5+ years of relevant experience (preferred)