Vacancy for Statistical Programming Professionals at GCE Solutions | 20 posts

GCE Solutions is a global clinical research organization (CRO) and IT business solutions provider. We were incorporated in March 2006 located in Alpharetta, GA, and then shortly expanded to another location in Bloomington, IL. GCE initially focused solely on IT business solutions and soon turned into a Biometrics focused CRO. Majority of our business has been directed towards CRO services since late 2007, but we have certainly not abandoned our IT business solutions sector. We have assisted in clinical development in the pharmaceutical, biotechnology, and medical device industries with various programming, statistical, and consultancy tasks among an array of therapeutic areas and phases. Alongside our CRO success, we have implemented IT solutions regarding IBM software (we are a Premier IBM Business Partner), Microsoft software, and network enhancements.

Post : Statistical Programming Professionals

No of Posts : 20

Job Description

Advanced knowledge of / experience with SAS and other relevant programming software.
Proven experience in development of advanced MACROs with high programming efficiency.
Must have experience in Safety and Efficacy.
Strong programming and problem-solving skills.
Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent)
Must have expertise in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL.
Skilled in SAS programming, merging SAS datasets, preparing data, producing and validating reports, SAS formats, and managing data.
Must have working knowledge in using report generating procedures like PROC CONTENTS,PROC PRINT, PROC REPORT, PROC TABULATE, PROC FORMAT, PROC FREQ, PROC UNIVARIATE, PROC SUMMARY, and PROC TRANSPOSE.
Working knowledge of database design/structures and basic statistics.
Working experience in pooling analysis datasets across multiple clinical studies (or equivalent)
Should have experience in phases I- IV of Clinical trials, Integrated Summaries of Safety (ISS) and Integrated of Efficacy (ISE).
Good understanding of global clinical trial / project practices, procedures, methodologies.
Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH).
Intermediate knowledge of office tools.
Should have experience with SDTM Implementation and ADaM implementation according to CDISC Standards.
Must have strong written/verbal communication skills.
Fluent English (oral and written).

Additional Information
Experience : 3+ years
Qualification : B.Sc
Location : Ahmedabad
Industry Type : Pharma/ Biotech/ CRO/ IT
Functional Area : Statistical Programmer
End Date : 10th October, 2018

Walk in Interview
Date: 29th September ,Time: 9 AM onwards
Venue: The Metropole RTO Circle Near Subhash Cir Corner, Ahmedabad, Gujarat 380027