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Study leader/ project manager - RWE/ RWD /EHR /Claims – (F/M)

Paris, Paris, France

Job 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 ground-breaking 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.

Thanks to our business growth, Cerner Enviza is looking for a new talented Study leader / Project Manager for real world evidence generation focusing on secondary data (claims, electronic health records, linked data).
In this role, you will have the opportunity to go beyond local data and manage studies with one or multiple existing data sources across all continents, ensuring that projects are scientifically aligned with the study objectives and delivered timely, within budget, and with the right allocation of resources. The position is highly international, reporting to the Associate Principal in the RWD and Analytics team.

MISSION
  • Be the client’s main point of contact throughout the entire study execution, under the supervision from a more senior team member.
  • Manage the execution of real world studies involving secondary data, where usually team members from diverse backgrounds participate: medical doctors, pharmacists, epidemiologists, oncology specialists, data scientists, statisticians, regulatory experts, medical writers, etc.
  • Proactively manage the client relationship - kick-off, regular follow up via teleconferences, day-to-day management, results presentations – ensuring client satisfaction
  • Plan study execution, milestones, and timelines, and assembling the multi-disciplinary team adapted to the project with the support from a more senior team member
  • Provide scientific or methodological input to build robust study methodologies adapted to client needs and objectives
  • Be responsible for all the study materials associated with a project, such as protocol, reports, manuscripts, posters, and abstracts with the help of more junior members of the team
  • Manage the relationship with data providers
  • Oversee the data access process and manage submissions when needed
  • Plan and develop data analysis with the support of the multi-disciplinary team
  • Guide and monitor the research analysts and data analysts within the project and to contribute to their development
  • Present results and recommendations to clients
  • Sporadically, be involved in activities related to proposal development (study design, methods, analysis, budget, timelines) and on strategic workstreams fitting your background and experience.
  • Sporadically, participate in the generation of new opportunities with new and existing clients in collaboration with our Client Partners/Business Development team
  • Collaborate in the growth of more junior team members by providing appropriate feedback, sharing knowledge and contributing to a collaborative work environment where people’s background/skills are valued, respected and continuously improved.

Working Environment

Hybrid or Remote

This position offers a Hybrid or Remote working environment. Meaning if you live within a metro area of a Cerner office, you will split working time between a Cerner office and remote. If you are not within a metro area of a Cerner office, you can live and work in your current geographical location and work primarily remote. #LI-Hybrid #Remote

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Because It's Personal

Time: 2:57

Additional Information

Working Environment Hybrid or Remote
Relocation Assistance Available for this Job: No

Qualifications

QUALIFICATION
  • You are flexible, curious and passionate by science with a strong background in healthcare/ life sciences (Epidemiology, Statistics, Pharmacy, Medicine, Biomedicine, Biology, Public health, , Pharmacoepidemiology, Health Economics, Data science, etc.).
    • Data-oriented profiles such as epidemiologists/ pharmacoepidemiologists, biostatisticians and data scientists will be preferred in this selective process, but we’re open to discuss with other candidates with proved experience in healthcare and matching the described profile.
  • You are able to understand big data and how to use it for solving problems related to human health space, having minimum 3 years conducting secondary data studies
  • You have strong knowledge with at least one real-world database (claims/EHR), and is able to discuss its pros and cons
    • Nice to have: if your knowledgeable about sources from one of the major markets in the secondary data domain (Europe, Japan, Taiwan, US, Israel, Nordics, etc.)
  • Professional fluency in English (C1 minimum)
  • You are client oriented with excellent ability to understand client objectives and needs
  • You have demonstrable client & project management skills
  • Excellent communication skills – able to distill issues, manage client expectations and act as a trusted advisor in a timely manner
  • Strong organizational skills, self-starter and fast learner, you react to change productively and display a solution-driven approach
  • You are flexible: if things do not go as planned, you adapt, and carry on
  • You are open to new ideas & innovative ways of working
  • You have the ability to inspire and motivate people within research teams

All employees must be legally authorized to work in the country where the position is located. Work visa sponsorship is not available for this position.


Cerner is a place where people are encouraged to innovate with confidence and focus on what is important – people’s health and the care they receive. We are transforming health care by developing tools and technologies that make it more efficient for care providers and patients to navigate the complexity of our health. From single offices to entire countries, Cerner solutions are licensed at more than 25,000 facilities in over 35 countries.

Cerner’s policy is to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Cerner is proud to be a drug-free workplace.
If you are an individual with a disability who is unable to use our online tools to search and apply for jobs, and need assistance or an accommodation in the recruiting process, please contact us by calling 866-434-1543 or by emailing CernerCareers@cerner.com.

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