Pro Business Services
Location
Vijayawada | India
Job description
Location : Vijayawada , Andhra PradeshÂ
Office timings : 1:30 Pm to 10 PM
Client details : Channelsoft IT services Pvt LtdÂ
Domain: Health Care (Clinical Trails)
About Channelsoft
Channel Soft is a pioneer in IT outsourcing and offshore software development business that envisioned and instigated the adoption of the flexible business practices that today enable our client companies to operate more efficiently and produce more value.
Currently in India we have employees around 550+ working on various technologies like java,.net , DB, BI, AWS and support team .
Office address : Nagarjuna nagar , near NTR university , Vijayawada .
Responsibilities For Clinical SAS Programmer:
• Creating and executing SAS edit check programs
• Validating edit check programs using standard validation practices and processes
• Creating, validating and executing SAS programs and macros
• Utilizing SAS programming skills to provide ad-hoc reports (external and internal) and participating in project meetings (internal and external)
• Assist in developing programming specifications and in creating program specific validation plans
• Identifying and implementing solutions for complex reporting needs
• 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 data cleaning/consistency checking programs to support internal applications for all therapeutic areas
• 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 and utilizing SDTM guidelines to create transfer datasets
• Participating in the development of data editing conventions, specification documents and Clinical Data Management (CDM) processes
• Contributing to, designing and maintaining a library of reusable code
• Leading and managing enhancements to current CDM systems and providing inputs in the implementation of new systems
• Working independently and efficiently with minimal 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 and communicating any changes in target date to appropriate personnel including Project Manager
• Keeping department head informed of progress as well as potential impediments
• Adhering to established processes and standards
• Reading, understanding and adhering to organizational Standard Operating Procedures (SOP)
• Assisting in establishing and enforcing departmental standards
• Maintain and review clinical programming SOPs and participating in the modification of company SOPs
• Working with internal staff to resolve issues and exploring new opportunities to add value to organization and departmental processes
• Helping others to achieve results and performing other duties as assigned
• Attending and participating in applicable company-sponsored training
Education :
• Bachelor's or Master's degree in computer science, life sciences or related field preferred
• SAS Certified Professional considered a plus
What we're looking for • 3 + years SAS programming experience in pharmaceutical related industry required (1 year with Master's degree)
• Experience working with CDISC, SQL 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 and understanding of medical and/or clinical trial terminology is desirable
• Proven ability in problem solving and 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, organizational skills and ability to project and maintain a professional and positive attitude
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