Job Description
Responsibilities
Provide statistical support for clinical studies
Participate in NDA/BLA activities
Provide statistical input to study protocols, develop statistical analysis plan
Assist in writing relevant sections of the clinical study report and publication
Monitor internal and CRO project activities including timelines, deliverables and resources
Ability to use R and or SAS to perform efficacy analyses and validate important data derivations when necessary.
Develop and implement department standards and lead process improvements
Minimum Requirements
PhD or MS in Biostatistics or Statistics;
2+ years of experience as statistician in Pharmaceutical or Biotechnology industries;
Candidate with Intern experience in the pharmaceutical industry will be considered
Good knowledge of statistical programming languages (including SAS, R);
Solid oncology and/or hematology experience
Experience with advanced study design or at least one NDA/BLA eCTDs or other global regulatory submissions
Experience as an independent lead statistician with responsibility for multiple studies or projects
Excellent interpersonal, leadership and communication skills and ability to work independently and collaboratively;
Knowledge of SDTM/ADAM
TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.Company Description
Hybrid remote