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SAS programmer

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

India

Offer summary

Qualifications:

BA/BS Degree preferred or equivalent experience, Master's/Bachelor's in Math, Statistics, Engineering, or related field, 2-4 years SAS experience in Pharmaceutical/CRO, Knowledge of programming languages like SAS Macros, SQL, Understanding of GCP and regulatory standards.

Key responsabilities:

Assist in clinical programming activities including data cleaning and reporting
Develop analysis data sets and implements SAP documentation
Provide timely communication about study processes and defects
Support validation for project requirements
Document processes for various programming tasks

Emmes Research Large https://www.emmes.com/

1001 - 5000 Employees

See more Emmes offers

Job description

Overview

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Clinical SAS Programmer is responsible for assisting the development of statistical programs and reports to analyze clinical trials in accordance to the project requirements

Responsibilities

Assists in preparation of clinical programming activities such as data cleaning, extraction and integration programs, web reporting programs, integrity reports, analysis datasets, CDISC SDTM and ADaM data mappings, CSR tables, listings and figures (TLF), ad hoc reports etc.
Assisting documentation of SAP, mock shells, randomization plan, analysis data specification and other documents within capacity of clinical programming.
Provides accurate, effective and timely communication of clinical study and defects to senior members of the team.
Understand the requirement of specific validation process for the project and help to document them.

Qualifications

BA/BS Degree preferred or equivalent years of experience in administrative work.
Requires a Master’s Degree/Bachelor’s Degree in Mathematics, Statistics, Engineering, Computer Science/Applications, Pharmacy, or any other similar type of qualification
At least 2-4 years of SAS experience as a Clinical SAS programmer in Pharmaceutical/CRO
Good knowledge of programming languages (SAS Macros, SQL etc.) with understanding of databases..
Good analytical skills with the ability to process scientific and medical data.
Knowledge in development, documentation, and testing of analysis data and programming code to meet regulatory and company standards.
Understanding of GCP principles and other regulatory standards in Clinical Research.
Good organizational and communication (written and oral) skills, ability to manage multiple tasks, ability to work with minimum supervision, as well as in a team environment and a desire to improve skills
professional speaking abilities for routine internal and/or external communication purposes.
Be willing to learn and adapt to new processes and procedures.

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