Clinical SAS Programmer

2 days ago

Hyderabad, India Statistics & Data Corporation (SDC) Full time

**Clinical SAS Programmer**

Statistics & Data Corporation (SDC), A global contract research organization (CRO) headquartered in Arizona, providing clinical trial solutions for pharmaceutical, biologic, and medical device/diagnostic companies since 2005. Our core expertise is strategic scientific consulting and clinical data services which include biostatistics, data management/EDC, and IRT/IWRS.

**Job Summary**

**Requirements**:
**Primary Responsibilities**
- Creating and/or reviewing data editing and export specifications
- Working directly with clinical data manager, and where needed with clinical project manager and other team members to ensure specifications are clear and accurate.
- Has a clear understanding of the contextual requirements for reporting outputs; and provides feedback
- Programming and testing data export programs in accordance with specific client needs
- Documenting all programming and validation efforts in accordance with Good Clinical Practices
- Monitoring data integrity throughout a given study
- Participating in project meetings (internal and external)
- Participating in the development of data editing conventions, specification documents and Clinical Data Management (COM) processes
- Contributing to, designing, and maintaining a library of reusable code
- Leading and managing enhancements to current COM systems and providing inputs in the implementation of new systems.
- Working independently and efficiently with mínimal input required from the manager. Reviewing timelines; and projecting estimates and target dates in conjunction with direct supervisor and project team
- Adhering to target dates for project timelines
- Communicating any changes in target date to appropriate personnel including Project Manager
- Keeping department head informed of progress as well as potential impediments
- Attending and participating in applicable company-sponsored training
- Comply with SDC's data integrity & business ethics requirements
- Perform other duties as assigned
- Adherence to all essential systems and processes that are required at SOC to maintain compliance to business and regulatory requirements

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

**Required Skills**:

- 3 years SAS programming experience in pharmaceutical related industry required
- Experience working with CDISC, SOL, and Relational Databases preferred
- Demonstrated programming skills required
- Working knowledge and solid understanding of database organization and how to extract data in order to generate listings and reports
- Proven ability in analyzing data
- Understanding of medical and/or clinical trialterminology is desirable
- Proven ability in problem solving
- Ability to work in group setting and independently; ability to adjust to changing priorities
- Excellent attention to detail and orientation toward meticulous work
- Strong interpersonal and communication skills, both verbal and written
- Strong documentation and organizational skills
- Ability to project and maintain a professional and positive attitude

**Education or Equivalent Experience**
- Bachelor's degree in computer science, life sciences or related field required
- SAS Certified Professional considered a plus

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