Overview
Quinten Health is recruiting a Biomedical Consultant to join the Healthcare team, working in close collaboration with Data Scientists, engineers, Biostatisticians, and Project Managers. You will be supported by Senior Biomedical Consultants.
Responsibilities
- Your key responsibilities will be :
- Working in collaboration with the team of data science engineers on delivery projects to :
- Assess the fitness of Real-World databases.
- Provide clinical and scientific input to support analytical work (e.g. modeling).
- Capturing clinical characteristics in real-world databases, including finding proxies for clinical events and / or scores, time windows for data capture
- Defining the target study population, outcome of interest, covariates, and confounders
- Providing code lists for diagnosis, treatments, procedures, etc…
- Structure the data to ensure the quality of the analysis from a medical point of view (e.g. capture and interpret chronic and acute diseases differently).
- Develop variable derivation strategies to extract a maximum of information from data (e.g. therapeutic escalation to measure a patient’s severity).
- Adapt the analytical strategy to align the results with the medical objectives of the project.
- Interpret the output of analyses, assess findings, and provide relevant insights based on existing literature.
- Write up results in reports and publications.
- Give input on the scientific aspects of projects, coordinating with data scientists, epidemiologists, statisticians, and project managers.
- Perform necessary administrative functions and additional tasks, as required.
- Contributing to the innovation and development activities of the organization to :
- Perform literature reviews on a therapeutic area or disease to identify and describe unmet needs, pathophysiology, standard of care tailored to the specific activity.
- Assess potential data sources and partnerships to support the development of disease and care models.
- Engage with scientific or medical KOLs to provide relevant insights and validation of internally developed disease and care models.
- Participate in company-sponsored training programs as required to ensure that skills are learned, maintained, and focused accordingly.
Preferred education and experience
- Medical, Pharm D degree, PhD or Master’s Degree in life sciences (-omics, physiology, cognitive etc.).
- Minimum of one year of relevant professional experience (e.g., in the pharmaceutical industry, medical writing, academic or clinical research, or health-related consulting).
- Knowledge on pharmaceutical industry, health regulation, and clinical practices is a must.
- Professional proficiency in English, written and spoken is a must.
- Ability to work both independently and as part of a team.
- Ability to effectively prioritize and manage multiple tasks and projects.
- Ability to make decisions and think strategically.
Additional Skills
- Experience in epidemiology is a plus.
- Basic knowledge of programming (e.g., R, Python, PySpark) is valued to facilitate dialogue around statistical analyses and the interpretation of tables and figures.
- Experience with claims databases or electronic health records (such as SNDS, CPRD, HES, sickness funds data, national or disease registries) is a plus.
- Knowledge of statistical and machine-learning methods is a plus.
- Experience on the analysis of -omics is a plus (RNA expression, genetic analyses etc.).