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Director, Product Management (R1065377) in Blue Bell, PA at IQVIA™

Date Posted: 5/18/2019

Job Snapshot

Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. IQVIA has approximately 55,000 employees in more than 100 countries, all committed to making the potential of Human Data Science a reality, and we are actively hiring.

Reimagine healthcare with us

At IQVIA, you will have the opportunity to build your career, while helping our customers drive human health outcomes forward. We dedicate our experience, resources and reputation so that you can drive your career and choose the path that best defines your development and success

At IQVIA, we look for the very best people, and then give them meaningful work to do. We don’t simply think about careers, we think about contributions.

ROLE SUMMARY

Your work as offering Director will be an integral part of IQVIA's RIM Smart (formerly RIM +) program that involves multiple work streams to create innovative next-gen regulatory the technology solution for the Life Sciences Industry (Pharma & Med Tech).


The RIM smart program includes multiple modules including several offerings that need to be organically developed from the ground up.
- Regulatory Content Management
- Product Registrations
- Publishing & Submissions
- Labeling management (brand new offering)
- Embedded workflows and Robotic Process Automation
- Machine translations 
- Regulatory Intelligence
- Integration to Quality and Safety systems

The Director, Product Management/Offering Management role will help drive design and development of multiple of these offerings(s) in working with product engineers and other groups within IQVIA.

You would be required to work with the senior execs on RIM Smart program day to day developing product strategy, reviewing requirements, ensuring requirements meet market demands and communicating our roadmap regularly. In addition, this role will be interacting with Sales and Marketing teams across U.S and Europe, presenting our solution/vision in RIM space in support of large deals in Top 30 pharma HQ.

RESPONSIBILITIES

You will be designing innovative product features based upon industry requirements for Life Sciences across all RIM smart including labeling, auto translation, next gen business process workflow and overall regulatory content management strategy along with:

  • Driving overall regulatory product strategy and work with clinical teams to drive auto translation
  • Providing subject matter expertise based on industry knowledge and experience
  • Supervising and contributing to the creation of high-quality user and functional specifications within an agile methodology
  • Working together with customers, services, and sales to understand business needs
  • Interacting with engineering team to drive high quality product feature implementation
  • Conducting market research and competitive analysis
  • Ensuring that test suite accurately tests defined requirements
  • Planning and preparation of related materials such as training materials and client User Acceptance Test materials, release notes, etc.
  • Delivering support to areas of the organization including: QA, Support, Professional Services, Marketing, and Sales

QUALIFICATIONS

  • Bachelor’s Degree
  • 10+ years’ experience in information technology and product development expertise  
  • Proven experience working in life sciences, healthcare, pharmaceutical industry
  • Regulatory Information Management know-how
  • Sound Content Management, Regulatory and eSubmissions knowledge, specifically RIM
  • Clinical trials software experience, specifically EDC, CTMS, IVR/IRT, eTMF  
  • Experience directing product managers, working with vendors, meeting industry subject matter experts and clients
  • Able to gather functional and user requirements, features and present to internal and external audiences
  • Verifiable experience managing products through design development and release of software products


#LI-RP1

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.  Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.



Job ID: R1065377