Clinical Programming

The Programming lead is responsible for data definition, processing, data integration and reporting for all clinical trials to ensure all databases meet business objectives. A secondary function is to work with vendors to ensure receipt of data.
This position is also responsible for providing professional expertise and leadership through leading departmental tasks and taking initiatives in improving Clinical Programming processes with focus on programming activities.
The SDTM Programming Lead Evaluates and makes recommendations related to inter- and intra-departmental processes in order to identify 
and implement efficiencies and quality improvement measures. 2-5 Yrs of related experience.
Education Required: Bachelor’s or higher degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience. 
Experience Required: More than 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer.
Experience in SDTM and ADaM (as applicable), acquainted with CDISC guidelines and requirements.
Experience Preferred:   Specialized or Technical Knowledge Licenses, Knowledge of standard Windows programs (Word, Excel, Access, and Outlook). Company/Industry Related Knowledge: In-depth SAS Programming knowledge.
Understanding of clinical data and pharmaceutical development.
Job-Specific Competencies:
1.      Good oral and written communication skills in English.
2.      Interpersonal communications skills.
3.      Ability to effectively work in a global environment.
4.      Ability to effectively interact with and influence others without direct reporting relationships.
5.      Professional accuracy and integrity.
6.      Ability to work under pressure and multitasking.
7.      Innovation driven and open for change.