As a Senior Project Manager, you will lead a multidisciplinary project team to conduct real-world (observational) patient studies for our clients, including pharmaceutical companies, medical device manufacturers and medical researchers.

Your main responsibilities within a multidisciplinary team (pharmacists, statisticians, engineers, sales representatives) includes:

• Overseeing the conduct of prospective observational studies coordinating project teams of 2-4 people: literature review, study design, development of protocol and questionnaire, regulatory procedures, data collection, in-depth analysis, development of study report, and presentation of results to the client.

• Ensuring effective client relationship management throughout projects while delivering qualitative, ethical, and scientific consulting.

• Participating in leading scientific committees and supporting scientific communications.

• Coordinating the writing and publication of posters and scientific articles in reference journals or medical conferences.

• Identifying, selecting and managing external providers.

• Contributing to the professional development of team members and sharing knowledge with the project team and the extended team

• Demonstrating RWE expertise to contribute to the development of proposals with the business development team

• Contributing to the development of new methodologies: patient-generated health data, data linkage (connected devices, health insurance data…).

• Collaborating with other teams to improve Carenity’s offering for patients, collaborators, members and clients.

These responsibilities are not exhaustive and can be adapted according to the candidate’s profile and development aspirations: at Carenity, each employee’s career is personalized!

Prerequisites:

• At least 3/5 years of experience in management of Real-World Evidence/ Non-Interventional studies (preference studies, registries/ databases, epidemiological studies, patient studies …) or Clinical trials, preferably in a CRO or in a consulting company.

• Fluent in French and English (written and oral)

• Client oriented, with excellent communication skills and the ability to build trusted relationships with clients

• Excellent analytical, writing and synthesis skills, with the ability to convert data into meaningful insights

• Autonomy, proactivity, and organizational skills.

• Mastering of Microsoft Office tools

• Understanding of statistical principles/statistical knowledge

• Graduate of a top-ranking engineering school and/or a master’s degree or PhD in statistics, mathematics, biology, epidemiology, public health or pharmacy.

Nice to have:

• Knowledge of the regulatory framework for health studies

• Knowledge of requirements of HTA bodies regarding RWE and/ or experience submitting RWE data to HTA bodies in different countries

• Proficiency in R

• Proficiency in one or more data visualization tools (e.g., Power BI)

• Proficiency in one or more additional languages.

• You love having fun with your colleagues: afterworks, games, etc.