Clinical SAS Programmer Information

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Accenture India

Accenture is a global management consulting, technology services and outsourcing company, with approximately 259,000 people serving clients in more than 120 countries. Combining unparalleled experience, comprehensive capabilities across all industries and business functions, and extensive research on the world’s most successful companies, Accenture collaborates with clients to help them become high-performance businesses and governments. The company generated net revenues of US$27.9 billion f... Read More

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Clinical SAS Programmer

We are looking at young, enthusiastic Clinical SAS Professionals for Pharma Across Levels we have for our Mumbai & Bangalore Locations. Qualification : Any Desired Skills: Graduate with 2 to 6 years of experience in Clinical SAS Programming Should be an expert in Generating Reports. Should be an expert in TLFs (Tables, Listings & Graphs) Job Profile Create and/or annotate and review tables and listings mocks; ensure internal consistency within and among tables and listings; ensure that all CRF fields are displayed on listings. Review clinical data for outliers, invalid and illogical data points. Interact with Clinical Data Management (CDM) to resolve data issues. Must be able to use univariates, frequencies, Proc Transpose, and macros, including modifying existing macros and writing macros. Follow all pertinent SOPs and guidelines concerning programming and the change control management of all files generated by the Biometrics Programming group. Program routine data displays, such as data listings, in accordance with approved statistical analysis plan and shell displays for clinical research studies. Code is to be written using Base SAS programs, SAS procedures, or standardized macros. Perform data checks as needed to understand structure and content of data. Write and compare independent QC programs to verify the output generated for data displays. Coordinate QC project teams on large projects, which includes training and delegation of QC work. Create and maintain standard QC documentation. Maintain tables and listings binders, if applicable, which includes a hard copy of the latest versions sent to the client. Send tables and listings to clinical writers and clients, which includes printing, collating, and filling out appropriate shipping paperwork. Attend both client and team meetings when needed. Respond to non-statistical questions from Clinical Writing and from clients. Assist in establishing departmental processes, interaction with other departments, training of staff, and other departmental administrative tasks. Oversees all the team resources in the work. Provide technical and/or configuration, best practices to team resources as required Oversee execution of Quality Control and discrepancy management for outputs Assist in training for new resources and as a part of continuous improvement Should be an expert in working on datasets such as DM AE LB VS EG MH etc Should have good experience in MACROS Should possess good written and verbal communication skills

Other Job Information

Vacancy type:	Full Time	Contact Mode:	not provided
Fax:	not provided	Contact Name:	Swetha
Job Duration:	not provided	Phone:	not provided
Email:	swetha.chidanand@accenture.com