PHARMACOVIGILANCE SPECIALIST

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Share job PHARMACOVIGILANCE SPECIALIST - Contract - Lawrenceville/New Brunswick - $47.00 - $57.00/hr. The final salary or hourly wage, as applicable, paid to each candidate/applicant for this position is ultimately dependent on a variety of factors, including, but not limited to, the candidate's/applicant's qualifications, skills, and level of experience as well as the geographical location of the position. Applicants must be legally authorized to work in the United States. Sponsorship not available. Our client is seeking a PHARMACOVIGILANCE SPECIALIST in Lawrenceville/New Brunswick. Role Description 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 WWPS 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 WWPS. Responsibilities include, but are not limited to the following: 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 • 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/WWPS initiatives including relevant insights to facilitate decision-making process • Assess and interpret the process impact of new PV tools and processes Skills & Requirements Skills/Knowledge Required: • Life Sciences, Information, or similar background (Bachelors, Masters) • 5+ years Drug Safety/Pharmacovigilance experience • Advanced Tableau, Spotfire, Power BI, SAP Business Objects (BO) skills with 5+ years of development experience • Databases (Postgres, Oracle, MS Access, Impala, SharePoint List etc.) • Programming languages (SQL, VBA, Python etc.) • Reporting platforms and services (Cognos, SAP-Business Objects, Power BI etc.) • 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 Benefits/Other Compensation This position is a contract/temporary role where Hays offers you the opportunity to enroll in full medical benefits, dental benefits, vision benefits, 401K and Life Insurance ($20,000 benefit). Why Hays? You will be working with a professional recruiter who has intimate knowledge of the industry and market trends. Your Hays recruiter will lead you through a thorough screening process in order to understand your skills, experience, needs, and drivers. You will also get support on resume writing, interview tips, and career planning, so when there's a position you really want, you're fully prepared to get it. Nervous about an upcoming interview? Unsure how to write a new resume? Visit the Hays Career Advice section to learn top tips to help you stand out from the crowd when job hunting. Hays is committed to building a thriving culture of diversity that embraces people with different backgrounds, perspectives, and experiences. We believe that the more inclusive we are, the better we serve our candidates, clients, and employees. We are an equal employment opportunity employer, and we comply with all applicable laws prohibiting discrimination based on race, color, creed, sex (including pregnancy, sexual orientation, or gender identity), age, national origin or ancestry, physical or mental disability, veteran status, marital status, genetic information, HIV-positive status, as well as any other characteristic protected by federal, state, or local law. One of Hays' guiding principles is 'do the right thing'. We also believe that actions speak louder than words. In that regard, we train our staff on ensuring inclusivity throughout the entire recruitment process and counsel our clients on these principles. If you have any questions about Hays or any of our processes, please contact us. In accordance with applicable federal, state, and local law protecting qualified individuals with known disabilities, Hays will attempt to reasonably accommodate those individuals unless doing so would create an undue hardship on the company. Any qualified applicant or consultant with a disability who requires an accommodation in order to perform the essential functions of the job should call or text 813.336.5570. Drug testing may be required; please contact a recruiter for more information. #LI-DNI

Created: 2024-11-09