Job Opportunities

Independently create, execute, maintain, and validate programs that transfer data across multiple data management systems or operating systems, combine data from a variety of sources and structures, generate and store summary data from a variety of sources generate reports or combine multiple databases.

Serve as a project lead and oversees work of other programmers on team.

Manage assignments to meet timelines and deliver high quality work, being familiar with any relevant contractual obligations or limits.

Assume leadership responsibility as a contributing member of a multidisciplinary clinical trials project team, communicating actively and frequently with other team members as needed.

Demonstrate a good understanding of the role of the programmer in the overall process.

Provide general infrastructure support to the Biostatistics Department. Examples include presentation / teaching at Department meetings, contributing to other general department documents or policies, and assisting with Biostatistics web page development.

Increase knowledge base and professional skills in areas including programming, technology and techniques, clinical trials, and the pharmaceutical industry.

Develop SAS macros, templates and utilities for data cleaning and reporting.

Communicate with an internal team to create deliverables for pharmaceutical and biotechnology clients.

Implement analyses specified in the protocol or the Statistical Analysis Plan (SAP) while working with the project statistician.

Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy.

Write SAS programs to generate tables, listings, and figures and analysis datasets.

Work in tandem with Biostatistics and Data Management member on various clinical projects.

Identify and edit checks per the data validation plan or data management plan.

Validate the programmed analysis datasets, tables, listing and figures.

Communicate with programming and statistics leads.

Utilize SAS programming skills within protocol team and perform all programming required for clinical trial analysis and reporting.

Develop SAS coding and table templates for preparing, processing and analyzing clinical data.

Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.

In this role you will partner with Product Security & Security Engineering teams for detecting threats to Snowflake’s Cloud Infrastructure and the Snowflake platform Work closely with stakeholders to understand the use-cases and identify focus areas with the highest potential for impact

Define and analyze metrics that will in-turn inform the key drivers for decision making & operational efficiencies

Analyze large amounts of messy data, work on data quality, uncover actionable insights and present them in a compelling manner

Provide technical & thought leadership designing and implementing machine learning techniques
Responsibilities for this position include support to System Administrators and software engineering during the development of a new system by installation, configuration, patching, and maintenance of databases

The position includes participation in the program's focus on smoothing the transition from system development to operational readiness within the program's lifecycle

Performs database software installations, configurations, patching, and upgrades on RedHat and Windows operating systems

Maintains databases in accordance with established policies, procedures, and service level agreements

Administers database in both a VMWare virtualized environment and bare metal servers possibly involving containerized applications

Troubleshoots problems associated with the assigned Enterprise system(s) collaborating with the SysAdmins and Software

Works to automate deployment of database related repetitive tasks and maintain them
Experience with requirements gathering, design and specification development of eCRFs, edit checks, and understanding of database structures and programming languages

As a Senior Clinical Database Programmer, you will be responsible for delivering quality EDC trial configurations for leveraging VEEVA ECD

In addition, as the Senior Clinical Database Programmer you will perform Quality Control of configured projects for activities that they did not perform the development/configuration

You will also provide consulting services that may include user acceptance testing (UAT) of EDC systems, global library/standards development, and report quality control