Job Description
Hi,
About US :
Accenture is a global management consulting, technology services and outsourcing company, with more than 246,000 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.
Accenture does not discriminate on the basis of race, religion, color, sex, age, non-disqualifying physical or mental disability, national origin, sexual orientation, gender identity or expression, or any other basis covered by local law
Position : Clinical SAS Programmer/ (SME/TL/AM Level)
Job Location : Mumbai
Shift : Day Shift
Job Profile :
- Create SAS datasets of clinical data from Biometric databases; create status and efficacy datasets; create project specific macros and formats; load client data from other platforms; prepare data to be sent to clients.
- Create summary tables, listings and graphs as per statistical analysis plan.
- QC summary tables, listings and graphs as per statistical analysis plan.
Responsibilities/Authorities
- 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 SOP"s 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,
- Send tables and listings to clinical writers and clients, which includes printing, collating, and filling out appropriate shipping paperwork.
- 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.
Skills Required:
* 3-10 Years of relevant experience in to Clinical SAS
* Good communication skills
If your interested rewart back with your updated cv,current ctc,expected ctc & Notice period ASAP..
If profie is not suitable or if you have already applied for this position please ignore the mail,
Please forward the mail to your friends,collegues & suitable candidates.
Thanks & Regards
Varsha . |Accenture Services Pvt Ltd
About US :
Accenture is a global management consulting, technology services and outsourcing company, with more than 246,000 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.
Accenture does not discriminate on the basis of race, religion, color, sex, age, non-disqualifying physical or mental disability, national origin, sexual orientation, gender identity or expression, or any other basis covered by local law
Position : Clinical SAS Programmer/ (SME/TL/AM Level)
Job Location : Mumbai
Shift : Day Shift
Job Profile :
- Create SAS datasets of clinical data from Biometric databases; create status and efficacy datasets; create project specific macros and formats; load client data from other platforms; prepare data to be sent to clients.
- Create summary tables, listings and graphs as per statistical analysis plan.
- QC summary tables, listings and graphs as per statistical analysis plan.
Responsibilities/Authorities
- 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 SOP"s 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,
- Send tables and listings to clinical writers and clients, which includes printing, collating, and filling out appropriate shipping paperwork.
- 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.
Skills Required:
* 3-10 Years of relevant experience in to Clinical SAS
* Good communication skills
If your interested rewart back with your updated cv,current ctc,expected ctc & Notice period ASAP..
If profie is not suitable or if you have already applied for this position please ignore the mail,
Please forward the mail to your friends,collegues & suitable candidates.
Thanks & Regards
Varsha . |Accenture Services Pvt Ltd
Salary: Not Disclosed by Recruiter
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: R&D
Role: Bio-Statistician
Desired Candidate Profile
Education:
Please refer to the Job description above UG - B.Sc - Any Specialization, Statistics, Any Graduate - Any Specialization
PG - Any Postgraduate - Any Specialization, M.Sc - Any Specialization, Statistics
Doctorate - Doctorate Not Required
PG - Any Postgraduate - Any Specialization, M.Sc - Any Specialization, Statistics
Doctorate - Doctorate Not Required
Company Profile
Accenture is a global management consulting, technology services and outsourcing company, with approximately 261,000 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 for the fiscal year ended Aug. 31, 2012.
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