Pay: 630 day
Location: fully remote
12 month Contract
Skills: Pharmaceutical experience, Proficient in statistical programming languages/software such as SAS and/or R, real-world evidence studies
The RWE Statistician is involved in planning, conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database), and/or large database .
The Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for real world evidence studies.
The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs.
Study Design and Analysis
Operate in collaboration with scientist in design studies and write protocols for the conduct of research projects.
Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created.
Collaborate with data sciences in the planning and implementation of data quality assurance plans.
Maintain currency with respect to statistical methodology, maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.
Influence team members regarding appropriate research methods
Perform peer-review of work products from other statistical colleagues.
Communication of Results and Inferences
Collaborate with team members to write reports and communicate results.
Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.
Support responses to regulatory queries and/or regulatory interactions.
Therapeutic Area Knowledge
Understand disease states,competitive landscapes, and regulatory environment in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.
Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training.
Statistical leadership and Teamwork
Introduce and apply innovative methodology and tools to solve critical problems
Merge scientific thinking and business knowledge to identify issues, evaluate options and implement solutions.
Minimum Qualification Requirements:
Qualified Statistician (MSc, Ph.D). in Statistics OR Biostatistics
Proven experience in conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database), and/or large database
Prior experience in Rheumatology, Dermatology, or Gastroenterology would be an added value (but not mandatory)
Other Information/Additional Preferences:
Proficient in statistical programming languages/software such as SAS and/or R
Able to work in a virtual environment
Teamwork and leadership skills
Technical expertise and application with working knowledge of experimental design and statistical analysis
Self-management skills with a focus on results for timely and accurate completion of competing deliverables
Creativity and innovation
Demonstrated problem solving ability and critical thinking
If you are interested please apply or send your CV to
Employment Type Contract
Advertiser Type Agency