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

发布日期: 9/18/2019

职位快速浏览

  • 员工类型:
    Full-Time
  • 地点:
    Blue Bell, PA
  • 职位类型:
  • 经验:
    Not Specified
  • 发布日期:
    9/18/2019
  • Job ID:
    R1065377

职位描述

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

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
 

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Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

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