Clinical Data Specialist

Azenta Life Sciences

2d•$107,000 - $134,000•Remote

About The Position

Azenta, Inc. is seeking a Clinical Data Specialist in Burlington, MA. This role involves performing clinical database design and management, data maintenance, and SOP management for structured workflows in clinical data processing. The goal is to ensure consistent client-interfacing data delivery and well-documented audits. The position may be located anywhere in the United States.

Requirements

A master’s degree (U.S. or foreign equivalent) in Bioinformatics, Biology, or related field.
Three years of experience in a bioinformatics-related occupation in the life sciences industry.
2 years of experience using clinical research workflows and SOP maintenance systems.
3 years of experience using R or Python to analyze next generation sequencing (NGS) data and perform data maintenance work.
3 years of experience designing and implementing NGS data analysis pipelines and solutions.
2 years of experience working in a CLIA-regulated environment.
3 years of experience working with different computational systems including AWS cloud and Linux servers.

Nice To Haves

3 years of preferred service provider experience interacting with clients to explain data analysis workflow and output.

Responsibilities

Perform clinical database design and management, data maintenance, and SOP management for structured workflows in clinical data processing and readily prepare for consistent client-interfacing data delivery and well-documented audition.
Review data transfer agreements with clients and perform internal and external database design and maintenance including clinical information tracking, documentation, reconciliation, result data integration with structured formats customized for different analysis workflows or platforms.
Evaluate different cloud-based data transfer and storage systems based on AWS and their compatibility in data analysis and delivery workflow with IT/clients to facilitate efficient turnaround of clinical data processing and cost savings.
Maintain audit-readiness of documentation through conformance to procedures and applicable data standards by consistently reviewing and tracking data processing-related workflows with related teams and reporting back any deviated workflow findings.
Write and review standard operating procedures of different Bioinformatics workflows and clinical data reconciliations.
Perform data analysis for different types of NGS projects with a focus on clinical and pre-clinical related services.
Test and develop pipelines for custom analysis requests.