C08 - MEDICAL AND REGULATORY AFFAIRS / PHARMACOVIG - PHARMACOVIGILANCE SPECIALIST

Pharmacovigilance SpecialistJob Number : 25-03625 Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Pharmacovigilance Specialist for our client in Lawrenceville, NJ. ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity! Position Overview : Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence – JD The Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence is responsible for successful execution, and close-out of activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regulatory reporting efforts in line with the overall PS needs. The PV Analytics and Reporting Specialist reports to the Senior Manager, PV Analytics Center of Excellence, within Global Biostatistics & Data Sciences. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting / visualization experience to drive successful servicing of information needs across PS. Responsibilities : Data Analytics and Reporting Build and continuously improve data analytics through supporting models that provide insights into efficiency, quality, stakeholder feedback, and key performance indicators to drive timely and informed decision making Maintain and develop reporting databases and analytics applications in environments such as Excel, Tableau, Power BI, SAP Business Objects and / or other Client environments Leverage internal data systems and tools to efficiently maintain data and reporting processes to minimize manual data retrieving Liaison with validation team to create validation test script, validation plan, validation summary report and test scripts. Contribute to qualitative and quantitative research projects through collaboration with data trends from cross-functional teams (Pharmacovigilance, Epidemiology, etc.) Utilize data analysis tools to aggregate and analyze data to make actional recommendations and answer key business questions Run and maintain reports regarding activities, outcomes, and be prepared to deliver presentations to management team on a regular and ad-hoc basis Collect data for monthly reports and quarterly reviews regarding activities, outcomes, and trends of the Advisor team Continually remain apprised of the constantly changing landscape of the healthcare industry and any impacts it may have to our Analytical programs and reporting mechanisms Analyze key stakeholder complaints, address rapidly, and discuss with applicable functional leads to collaborate and propose impactful and realistic solutions Maintain data integrity and traceability across the transformation lifecycle from the Source to Target Support program and project team activities required to implement innovation initiatives. Contribute to the management and prioritization of process improvement and innovation initiatives Define and provide metric reporting and data analysis for GBDS / PS initiatives including relevant insights to facilitate decision-making process Assess and interpret the process impact of new PV tools and processes Required Skills : Life Sciences, Information, or similar background (Bachelors, Masters) 5 years Drug Safety / Pharmacovigilance is nice to have. Advanced experience with creating reports in SAP Business Objects Advanced Tableau or Power BI experience in creating interactive dashboards Advanced SQL experience for data querying Knowledge and application of commercial coding dictionaries (MedDRA, WHO Drug) Ability to organize / curate data and see big picture from scattered pieces of information Knowledge of taxonomies, ontologies, and other knowledge management constructs Analytical and strategic thinking skills required Strong PowerPoint, Word, and Excel Skills Knowledge of Validation processes and associated documentation. Excellent verbal, writing, presentation, and project management skills Strong strategic orientation with ability to translate into operational priorities and plans Ability to promote cooperation and commitment within a team to achieve goals and deliverables. Ability to resolve complex problems and manage difficult stakeholder situations Ability to lead the development of critical path analyses and support scenario planning Promotes and practices effective pro-active decision-making, ensuring timely coordination and dissemination of information Demonstrated ability to work on multiple projects Strong willingness to collaborate with cross-functional partners Flexible, team member with positive attitude, friendly demeanor, ability to prioritize projects and balance competing priorities Confidentiality and integrity are required If hired, you will enjoy the following ECLARO Benefits : 401k Retirement Savings Plan administered by Merrill Lynch Commuter Check Pretax Commuter Benefits Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO If interested, you may contact : Jane Bautistafroilyn.bautista@eclaro.com3322060772Jane Bautista | LinkedIn Equal Opportunity Employer : ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.