ECLARO
Pharmacovigilance (PV) Analytics and Reporting Specialist
ECLARO, Lawrenceville, New Jersey, United States
Pharmacovigilance (PV) Analytics and Reporting Specialist
Be part of a company that delivers life-changing healthcare solutions. ECLARO is seeking a
Pharmacovigilance (PV) Analytics and Reporting Specialist
for our client in
Lawrenceville, NJ .
Position Overview:
Responsible for the successful execution and close-out of activities aligned with the vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function.
Contributes to the development, implementation, and execution of scientific, operational, and regulatory reporting efforts.
Reports to the Senior Manager, PV Analytics Center of Excellence within Global Biostatistics & Data Sciences.
Uses life sciences strategy, leadership, and reporting/visualization experience to service information needs across PS.
Responsibilities:
Build and improve data analytics using models that provide insights into efficiency, quality, stakeholder feedback, and KPIs.
Maintain and develop reporting databases and analytics applications in environments such as Excel, Tableau, Power BI, SAP Business Objects.
Leverage internal data systems to maintain data and reporting processes efficiently.
Collaborate with validation team to create validation test scripts, plans, and reports.
Contribute to research projects through data trend analysis from cross-functional teams.
Use data analysis tools to make actionable recommendations and answer business questions.
Prepare reports on activities and outcomes; deliver presentations to management.
Collect data for monthly reports and quarterly reviews.
Stay informed about changes in the healthcare industry affecting analytical programs.
Address stakeholder complaints and collaborate on solutions.
Ensure data integrity and traceability throughout the lifecycle.
Support program activities for innovation initiatives.
Contribute to process improvement and innovation prioritization.
Define and provide metric reporting for GBDS/PS initiatives.
Assess the impact of new PV tools and processes.
Minimum Requirements:
Background in Life Sciences, Information, or similar (Bachelors, Masters).
5+ years in Drug Safety/Pharmacovigilance preferred.
Advanced skills in SAP Business Objects, Tableau or Power BI, SQL.
Knowledge of MedDRA, WHO Drug coding dictionaries.
Strong organizational, analytical, and strategic thinking skills.
Excellent communication and project management skills.
Knowledge of validation processes and documentation.
Ability to work on multiple projects and collaborate effectively.
Confidentiality and integrity are essential.
If hired, you will enjoy benefits such as a 401k plan, pretax commuter benefits, and insurance options. To express interest, contact Jane Bautista at froilyn.bautista@eclaro.com or 3322060772.
#J-18808-Ljbffr
Pharmacovigilance (PV) Analytics and Reporting Specialist
for our client in
Lawrenceville, NJ .
Position Overview:
Responsible for the successful execution and close-out of activities aligned with the vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function.
Contributes to the development, implementation, and execution of scientific, operational, and regulatory reporting efforts.
Reports to the Senior Manager, PV Analytics Center of Excellence within Global Biostatistics & Data Sciences.
Uses life sciences strategy, leadership, and reporting/visualization experience to service information needs across PS.
Responsibilities:
Build and improve data analytics using models that provide insights into efficiency, quality, stakeholder feedback, and KPIs.
Maintain and develop reporting databases and analytics applications in environments such as Excel, Tableau, Power BI, SAP Business Objects.
Leverage internal data systems to maintain data and reporting processes efficiently.
Collaborate with validation team to create validation test scripts, plans, and reports.
Contribute to research projects through data trend analysis from cross-functional teams.
Use data analysis tools to make actionable recommendations and answer business questions.
Prepare reports on activities and outcomes; deliver presentations to management.
Collect data for monthly reports and quarterly reviews.
Stay informed about changes in the healthcare industry affecting analytical programs.
Address stakeholder complaints and collaborate on solutions.
Ensure data integrity and traceability throughout the lifecycle.
Support program activities for innovation initiatives.
Contribute to process improvement and innovation prioritization.
Define and provide metric reporting for GBDS/PS initiatives.
Assess the impact of new PV tools and processes.
Minimum Requirements:
Background in Life Sciences, Information, or similar (Bachelors, Masters).
5+ years in Drug Safety/Pharmacovigilance preferred.
Advanced skills in SAP Business Objects, Tableau or Power BI, SQL.
Knowledge of MedDRA, WHO Drug coding dictionaries.
Strong organizational, analytical, and strategic thinking skills.
Excellent communication and project management skills.
Knowledge of validation processes and documentation.
Ability to work on multiple projects and collaborate effectively.
Confidentiality and integrity are essential.
If hired, you will enjoy benefits such as a 401k plan, pretax commuter benefits, and insurance options. To express interest, contact Jane Bautista at froilyn.bautista@eclaro.com or 3322060772.
#J-18808-Ljbffr