Senior Biostatistician

hace 2 semanas

Madrid, Madrid, España Oracle A tiempo completo
Job Description

We are seeking a highly skilled Senior Biostatistician to join our team in the Real World Evidence projects. As a key player in the development of our ongoing activity related to patient-centric studies, you will be responsible for all statistical aspects of diverse projects, including experimental design, analysis, and statistical components of proposals.

Key Responsibilities:
  • 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;
  • Adept emergent analytical methodologies, tools and applications to ensure fit-for-purpose to answer the research question;
Requirements:
  • 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;
About Us:

Cerner Enviza 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.

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

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.

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