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. Were 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 PurposeThe Clinical SAS Programmer is responsible for assisting the development of statistical programs and reports to analyze clinical trials in accordance to the project requirementsResponsibilities:

• 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 Masters Degree/Bachelors 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.

CONNECT WITH US!Follow us on Twitter - @EmmesCROFind us on LinkedIn - Emmes#LI-Remote

Emmes