Job descriptionBachelor or Master (preferred) Degree in Statistics, Computer Sciences, Engineering, Pharmacy, biological sciences, IT, or related field.At least 5 - 6 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.Understanding of clinical data and drug development process, CDISC standards requiredStatistical Programming and SAS hand-on experienceClinical trials expertise with an understanding of data operations required for the reporting of clinicalGood understanding of ICH and regulatory guidelinesWorking knowledge of clinical data and relevant data standardsIs able to work with stakeholders across timezones under tight timelinesStrong written and oral communication skills, and time and project management skillsStrong competencies and interests for innovation and problem solvingProven ability to operate with limited oversightKnowledge of at least 1 Therapeutic Area