Senior Biostatistician - Patient Reported Outcomes (M/F)
Oracle
- France
- CDI
- Temps-plein
- Be Subject Matter Expert (SME) for biostatistics expertise in the team and for client discussions;
- Demonstrate good understanding of client business issues;
- Direct relationship with clients on Biostats matters at the proposal stage and all along the projects;
- Lead the biostatics activities in the team;
- Works synergistically within project team to provide statistical inputs in the development of the Biostat sections in the proposals (including sample size calculations and power estimation), and participate in bid defense meetings, if needed;
- Act as a primary point of contact for the study team on the Biostat activities/questions - communicate with team members regarding execution as it relates to types of analysis, timelines, budget, data quality, data analysis and interpretation of results;
- Provide expert statistical input, coordinate and/or develop Biostat sections in protocols, statistical analysis plans, table shells, and programming specifications and review and validate all needed deliverables;
- Analyses findings, interpretation and recommendations of final results to meet client needs;
- Participates in the presentation of results to clients;
- Supervise junior team members on projects;
- Provide statistical methods training sessions, coach, and mentor junior team members;
- Adopt emergent analytical methodologies, tools and applications to ensure fit-for-purpose to answer the research question;
- MSc or PhD in Statistics, Biostatistics, or related field;
- Ideally between 5-8 years of relevant experience in a bio/pharma/CRO;
- Fluency in English C2;
- Good knowledge in R tool and STATA;
- Good knowledge of programming logic, SQL and macro programming;
- In-depth knowledge of study designs, and statistical analysis;
- Excellent knowledge and applying of a wide variety of principles, theories and concepts in statistics and experimental design;
- Excellent communication skills - able to distill issues, manage client expectations and act as a trusted advisor in a timely manner;
- Ability to work effectively in a team in a fast-paced and dynamic environment;
- Experience in Preference studies and in PRO development and PRO validation studies would be a plus;
- Knowledge of clinical trials statistical methodologies, control arm studies/external control arm studies, regulatory' statistical expectations, in terms of propensity matching scores and statistical software packages would also be a plus;
- Which includes being a United States Affirmative Action Employer