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Senior SAS programmer

Remote:

Full Remote

Contract:

Full time

Experience:

Senior (5-10 years)

Work from:

India

Offer summary

Qualifications:

Master's/Bachelor's Degree in relevant field, Minimum four years of SAS experience, Knowledge of CDISC SDTM and ADaM, Familiarity with programming languages like SAS Macros, SQL, Understanding of GCP principles and regulatory standards.

Key responsabilities:

Design and develop SAS programs for clinical data analysis
Produce and validate various clinical programming deliverables
Contribute to Data Management and Validation planning
Ensure quality and timeliness of project activities
Participate in process improvement efforts

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 Senior Clinical SAS Programmer designs, develops, evaluates and modifies computer programs to analyze and evaluate clinical data, recognizes inconsistencies and initiates resolution of data problems. The Clinical Programmer typically creates programs using SAS to support the clinical research projects.

Responsibilities

Demonstrates technical proficiency to produce and/or validate all types of clinical programming deliverables such as data cleaning, extraction and integration programs, Web reporting programs, Integrity reports, randomization schedules, analysis datasets, CDISC SDTM and ADaM data mappings, interim and final statistical analysis reports, CSR tables, listings and figures (TLF), adhoc reports etc.
Develop and/or review programming specifications for various types of deliverables by applying SAS programming.
Contribute to the development of Data Management and Validation Plan, Statistical Analysis Plan,Table shells and other related documents within the capacity of clinical programming
Perform all other project and process related activities assigned by the supervisor, such as documentation of deliverables, timelines, client communication etc.
Contribute to on-going data quality improvement efforts within assigned projects using SAS and other proprietary software.
Demonstrates judgment in resolving problems.
Maintain quality and timeliness of assigned project activities and perform control checks with help of other team members for all the generated reports
Work with the programming teams and projects to ensure timeliness and quality of deliverables
Significantly contribute in implementing process improvement programs
Provide data on productivity, quality and timelines regularly to supervisor
Adheres to corporate standards for documentation and validation of statistical programming

Qualifications

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 four 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.
Knowledge of CDISC SDTM and ADaM models and data mapping process is desirable.
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.
Flexibility in time management
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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