Description
Primary Responsibilities:-Perform or oversee team in performing all SAS programming required for clinical trial analysis and reporting.
-Provide statistical programming expertise for project teams.
-Actively participate in developing the Statistical Analysis Plan.
-Design/develop SAS macros and other utilities to expedite SAS programming activities.
-Generate tables, listings, and graphs per protocol, Statistical Analysis Plan, and/or approved client request.
-Participate in statistical program validation and quality control activities.
-Actively participate in study team meetings.
-Interact with other departments, such as Clinical Operations, Project Management, and Data Management to ensure a high level of client satisfaction through successful execution of projects.
-Participate in review process of study documents such as the CRF, edit specifications written by Data Management, and Statistical Analysis Plans.
-Program data cleaning checks, as necessary, to facilitate Data Management's data cleaning activities.
-Participate in installation/validation of statistical software packages throughout the software development lifecycle.
-Develop and maintain the infrastructure for project files of SAS datasets and SAS codes.
-Mentor entry level statistical programmers.
-Ensure all programming activities and processes performed are conducted according to SDC's standard procedures and/or sponsor requirements.
-Adhere to all aspects of the SDC's quality system.
-Comply with SDC's data integrity & business ethics requirements.
-Perform other related duties incidental to the work described herein.
Required Skills:
-Strong analytical skills, with the ability to process scientific and medical data.
-Very strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat and SAS Macros. Basic understanding of SAS/Graph.
-Strong problem-solving skills.
-Able to work independently.
-Excellent knowledge of statistical programming.
-Proficient in manipulating and analyzing SAS data.
-Ability to identify data issues, present problems, and implement solutions.
-Capability of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues.
-Good organizational and time management skills, with the ability to multi-task.
-Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).
-Strong interpersonal communication and presentation skills.
Education or Equivalent Experience:
-Bachelor�s degree in computer science, statistics or other related, scientific field and five years of clinical trials experience; or an equivalent combination of relevant education and/or clinical trials experience.
To find out more about Real please visit www.realstaffing.com