Manager, Real-world Evidence Consulting - Paris, France - Cerner Corporation

Cerner Corporation
Cerner Corporation
Entreprise vérifiée
Paris, France

il y a 1 mois

Sophie Dupont

Posté par:

Sophie Dupont

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Description

Cerner Enviza an Oracle company is a leading global healthcare consulting firm and trusted advisor to many of the world's top pharmaceutical, biotech, and medical device & diagnostic companies.

By supporting the work of Cerner Enviza, you will work with world-class healthcare companies, helping them improve global access to medicines by connecting science and research.

Cerner Enviza is passionate about our people, our business, and our clients and is proud to foster a culture that contributes to the health and well-being of humankind.

Leading through innovation, we consistently challenge ourselves to discover and embrace new and creative ways to deliver exceptional insight for clients.


  • Together we leverage a diverse network of providers and data, expert research capabilities and actionable analytics to bring remarkable clarity to life sciences' most important decisions.
  • With ongoing and groundbreaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to work in Life Sciences and, with Cerner Enviza immersed in all of these, there has never been a better time to join us and make a difference to our clients and the lives of patients.
    Definition

The main role of this position is to provide scientific insights, ensuring scientific robustness and medical coherence throughout the study process, from the study proposal to the final report and publications, if any.


  • This person will play a double role supporting both the commercial side (as an expert in the offer, supporting the work of the business development team) and the operational side (in the process of proposal and study execution).
  • This person will be mostly dedicated to projects with primary data but may also participate in projects involving secondary data in the realworld evidence field (hybrid studies and others).
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PRIMARY RESPONSIBILITIES

In projects:

  • Typical mission is the conception of projects/proposals/study designs and provision of scientific insights of projects involving primary (chart reviews, directtopatient studies) and/or secondary databases (claims, EHR, registries, surveys) for realword studies from a scientific/medical point of view:
  • Playing a significant role in the development of a strong study proposal, including proposal writing
  • Adjusting and following up the study proposals when needed
  • For the projects won, being responsible for the definition of a clear study design, with robust and scientifically coherent methods, in close collaboration with other team members and the clients.
  • Being responsible for the medical/scientific inputs of all phases of the study delivery
  • Playing a significant role in the discussion and interpretation of the study results, in close collaboration with other team members, clients and (eventually) external partners.
  • Inputs for the development of the study report and publications, sometimes with a handson approach in the medical writing
  • Participation in discussions with clients, commercial meetings, and presentations
  • Gives specialist expert advice to internal stakeholders or external clients


  • Commercial activity

  • Understanding client needs, transforming them into clear objectives and robust study proposals
  • In studies involving primary data:
  • Responsible for guiding the team to ensure scientific coherence of the project and high-quality deliverables
  • Designs study methodology
  • Develops/validates study protocol, material and planning
  • Drives the biostat and analysis
  • Provide inputs to discussion of results and study report
  • Develops the appropriate storytelling to address clients' business issues
  • Develops and enhances analysis and recommendations
  • Participate in client discussions and presentations
  • Develops Study Reports
  • Develops publications (manuscripts, abstracts and posters)
  • Ongoing project team coaching
  • Consulting activities:
  • Even if this is not a typical mission, this person may be requested to develop consultancy activities that require scientific/medical knowledge:
  • Preparation and delivery of trainings/lectures to the internal team or for clients
  • Inputs to the development and execution of other Kantar offers, with participation in strategical projects and planning
  • Other activities
  • People management:
  • You will may be requested to manage some members of the team if needed
  • Project management:
  • Collaborate with the multiprofessional team to accomplish project objectives and timelines
  • Control and follow up commercial opportunities
  • Communicates with peers persuasively to gain cooperation for projects and activities within own functional area
  • Client management:
  • Responsible for client interactions when medical/scientific knowledge is required
    Working Environment:
  • Hybrid & Onsite: No Relocation Assistance OfferedThis position offers a Hybr
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