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Manager, Pharmacovigilance Data Analysis

Job in Clayton, Johnston County, North Carolina, 27520, USA
Listing for: Grifols, S.A
Full Time position
Listed on 2026-02-22
Job specializations:
  • IT/Tech
    Data Analyst
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Manager, Pharmacovigilance Data Analysis

NC-Clayton, US

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Summary

Provides operational support for global pharmacovigilance activities for Grifols investigational and marketed products. Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for project implementation and execution of system, including responsibilities for providing safety ongoing business support and ongoing improvements. Key interface with the IT system administrators to verify and test system changes ensuring that the system is compliant and meets business needs.

Responsibilities
  • Support drug safety applications with business administration tasks
  • Key expert to deliver solutions that are cost effective, sustainable, and meet business requirements
  • Develop training documentation and/or work instructions to determine methods and procedures
  • Coordination and management of signal management
  • Management of documentation describing PV applications use, which may include, but not limited to: SOPs, WP, User requirements, functional and/or technical specifications, process flow diagrams
  • Lead change management actions to assure PV team smoothly adapts to the new processes, as well as supporting the integration of a new application
  • Interact with Regulatory Authorities as it relates to safety database data transmission
  • Gathering, prioritizing, and planning improvements based on user requests, considering overall regulations to the business
  • Ensure data consistency and integrity within the safety database
  • Management and coordination of the updates in the database configuration of submission rules to Regulatory Authorities
  • Management and coordination of the updates in the database configuration of products and studies
  • Supervision and management of queries for data extraction used in different PV documents
  • Supervision and management of queries into the database to identify the interval and cumulative cases to be included in periodic reports
  • Supervision and management for obtaining case listings from the database for specific situations
  • Supervision and management of IT tickets needed for system compliance and improvements
  • Planning and prioritizing scheduled IT tickets
  • Project lead on the integration and establishment of the Grifols PV system
Knowledge, Skills, & Abilities
  • Proven Self-starter with strong work ethic and the ability to exercise good judgment.
  • Ability to work independently with minimum supervision.
  • Must be proactive, results oriented, and have strong attention to detail.
  • Strong organizational, analytical, and problem-solving skills with the ability to make structured decisions on a routine basis.
  • Strong interpersonal skills with the ability to interact and collaborate with personnel at all levels in a team environment.
  • Must possess strong technical writing and communication skills with ability to create and present design proposals, test scripts, execute training sessions and conduct effective meetings.
  • Ability to effectively prioritize and manage multiple tasks to ensure successful completion targeted deadlines
  • Proficient in Windows 7 and MS Office (Excel, PowerPoint, Visio, Word)
  • Familiarity with validation of computer systems and/or GMP environments is essential.
  • Knowledge of E2b (R2) and E2b (R3) is beneficial. Familiarity with Medical terminology, MedDRA, Who Drug is beneficial
  • Familiarity with reporting tools such as Business Objects is strongly preferred
  • Experience in team management.
  • Scientific expertise.
  • Planning and cross-functional collaboration skills and organized work habits.
  • Education or training in Information Technology or New Technologies, with knowledge of Systems Strategic Planning.
  • Databases and Spreadsheets…
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