Project Specialist

This position is responsible for configuration and deployment of IQVIA Investigator Portal technology solutions in accordance with the company’s/client’s strategic project plan. This individual will work collaboratively with their project team to ensure Investigator Portal technology deployments are aligned with user requirements. This individual will oftentimes act as an extension of our client’s clinical trial operations groups. 

Summary of Essential Job Functions

    Be an advocate and educator for our technology with sponsors, CROs, and sites
    Assist or lead in managing each trial’s directory of sites and members, including configuration of user permissions in accordance with customer requirements. 
    Setup and configure various aspects of the platform in accordance with customer requirements, including workflows, checklists, document library folder structure, reports, etc.
    Configure online training materials, quizzes, leaderboards, and other content and tools that facilitate trials. Understand protocols and develop site-friendly visit guides.
    Collect and analyze metrics around email activity, user feedback, cycle times, user login and website page views.
    Write and edit short news posts describing trial activities
    Prepare agendas and minutes for meetings, document key decisions and collaborate with team members
    Provide ongoing professional services support to clients as directed by project team
    Other duties as assigned

Minimum Experience Requirements

    Must have BA/BS degree, preferably in science/health care field, information systems, technology, business or equivalent degree and/or related experience.
    Prior experience at a biotechnology, pharmaceutical, CRO, clinical research, or healthcare technology company preferred.
    Experience working with and implementing SaaS technology solutions.

Skill Requirements

    Strong computer skills (i.e. HTML, CSS, Javasctipt (preferred), Microsoft Office (proficient in excel required), Mac OS, etc.)
    Knowledge of clinical trial process (preferred)
    Proven organizational skills and attention to detail
    Ability to handle multiple tasks and self-motivate when required to meet deadlines.
    Comfortable working in a global company with a team-oriented environment

Salary: 1400 € gross- Our offer to you may be higher based on your experience.

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 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.