Virtual Rheumatologist Jobs in Philadelphia, PA (NOW HIRING)

Purpose:

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.

Key Responsibilities:

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.

Regulatory Compliance

·        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 with at least 3 years of experience in the pharmaceutical industry

§  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

https://quantive.bio/