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Product Manager, Offering Development, IQVIA Regulatory Intelligence

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Primary Location: London, London, United Kingdom Additonal Locations: Amsterdam, Netherlands,NLD; Frankfurt, Germany,DEU; Oeiras, Portugal,PRT; Paris, France,FRA; Rome, Italy,ITA Full time R1219870

Job description

Responsibilitie

  • Works with Offering Owner to identify and scope future product lines by reviewing product specifications and requirements; appraising new product ideas and enhancements / changes to existing products   
  • Scopes, manages and executes offering development projects  
  • Determines customers' needs and desires by specifying the research needed to obtain market information
  • Works cross functionally to ensure that the offering meets customer needs 
  • Oversees and manages the resources assigned to support the offering development process  
  • Introduces and markets new products by developing time-integrated plans with sales, marketing and production 
  • Determines product pricing by utilizing market research data; reviewing production and sales costs; anticipating volume; costing special and customized products 
  • Engages independently with internal and external customers to define and describe product requirements 
  • Serves as point of contact for the development team to clarify requirements as needed 
  • Assesses market competition by comparing the company's product to competitors' products 
  • Defines product marketing communication objectives and messaging and provides source data

Required skills:

  • Experience with regulatory information and processes
  • Experience with tools used for regulatory, safety, clinical and quality compliance  
  • Demonstrated project management, program management, and team facilitation skills required
  • Experience working in the pharmaceutical, biotechnology or medical devices industry  
  • Demonstrated ability to operate effectively in a matrixed environment: Building and managing peer and management-level relationships through achievement of results, accountable to schedule, and allocation of resources and meeting customer needs 
  • Industry experience in a regulated or legal environment and clear understanding of government regulatory requirements preferred
  • Demonstrated understanding of the medical devices development process / product lifecycle and/or drug development / product lifecycle preferred 
  • Understanding of principles of database management, enterprise architecture, and systems analysis is preferred
  • Understanding of business rules and system rules creation and execution, to deliver data-led projects 
  • Excellent verbal and written communication skills required
  • Excellent interpersonal skills with the ability to interact and communicate effectively with all levels of management and staff across multiple departments and with service providers
  • Solution and results oriented
  • Self-motivated and able to take initiative and work independently and in a team environment

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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