Principal Statistical Programmer

Required Knowledge Skills and Abilities:

• Experience as technical team lead directly engaging clients and coordinating tasks within a programming team
• Indepth knowledge of applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Knowledge of statistics programming and/or clinical drug development process
• Advanced knowledge of R programming
• Base SAS SAS/STAT SAS Graph and SAS Macro Language
• Should have experience with SDTM Implementation and ADaM implementation according to CDISC Standards.
• Must have expertise in SAS/BASE SAS/MACRO SAS/STAT SAS/GRAPH SAS/ACCESS SAS/ODS SAS/SQL.
• Good organizational interpersonal leadership and communication skills
• Ability to independently manage multiple tasks and projects
• Ability to delegate work to other members of the SP team
• Excellent accuracy and attention to detail
• Ability to delegate work to other members of the SP team SPM
• Exhibits routine and occasionally complex problemsolving skills
• Ability to lead teams and projects and capable of managing at a group level
• Recognizes when negotiating skills are needed and seeks assistance.
• Ability to establish and maintain effective working relationships with coworkers managers and clients.

Responsibilities:

• Perform plan coordinate and implement the following for complex studies: (i) the programming testing and documentation of statistical programs for use in creating statistical tables figures and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically..
• Ability to interpret project level requirements and develop programming specifications as appropriate for complex studies.
• Provide advanced technical expertise in conjunction with internal and external clients and independently bring project solutions to SP teams and Statistical Programming department for complex studies.
• Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.
• Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.
• Estimate programming scope of work manage resource assignments communicate project status and negotiate/renegotiate project timelines for deliverables.
• Use and promote the use of established standards SOP and best practices.
• Provide training and mentoring to SP team members and Statistical Programming department staff.

Remote Work :

No