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ACL Digital (An Alten Group Company) hiring for Principal Statistical Programmer
Interested candidates can share their updated resume
Experience: 8 years relevant into SAS
Notice: Immediate/30 Days
Work location-Remote-India
The Principal Statistical Programmer of Statistical Programming is responsible for all statistical programming aspects of one or more clinical trials of drug development plans. The position ensures drug development plans are executed efficiently, with timely and high-quality deliverables. It is a blend of highly technical and leadership roles with a strong understanding of the drug development process and experience in regulatory activities.
Responsibilities:
The primary responsibilities will include:
· Implementation of statistical programming strategy related to innovation in technologies, automation, processes, and standards to maximize efficiency.
· Support the development and implementation of a programming ecosystem to enable successful project deliverables
· Review statistical analysis plans, mock-shells, database set-up specifications
· Validate or Review the Programming packages (includes the aCRFs, specifications and datasets, Define.XML and Reviewer's Guides (for both SDTM and ADaM)
· Develop department programming standards to meet business needs and regulatory requirements, enabling efficient and seamless production of deliverables
· Develop innovative solutions to standardize, automate and optimized efficiency and quality
· Proactively addresses project uncertainties to minimize risk and alerts or escalates the issue to the appropriate person (project team member, lead biostatistician, or management), identifies, communicates, and overcomes technical and interpersonal obstacles
· Development and maintenance of tracking systems, folder systems and archival of analysis
· Contributes strategies that allow multi-tasking or efficient implementation to reduce execution time to meet deadlines in fast-paced environment
· Build a team of programmers to support ongoing pipeline expansion
Job ID: 152704315
Skills:
SAS, Sdtm, Statistical Analysis, SDRG, programming specifications, CDISC compliance, ADRG, Define.XML, ADAM
Skills:
cdisc standards , R Programming, Sas Programming, Sdtm, Sas Macros, Statical Programming, Clinincal SAS Programming, Tlf, ADAM
Skills:
Base Sas, Sas Graph, Statistics programming, SAS Macro Language, Clinical drug development process
Skills:
markdown , cdisc standards , Java, Unix, SAS, Sdtm, Git, Linux, Python, Shiny, Define.xml, ADAM, R
Skills:
Machine Learning, statistical programming, Data Analysis