Clinical Research Systems – Bioinformatics Specialist

Saratoga Ascend

. Administer, configure, and migrate REDCap, CTDB, and other clinical research applications .

Posted 11/5/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in administering and configuring clinical research applications such as REDCap and CTDB, alongside strong scripting skills in Python, R, and SQL for data integration. Knowledge of NIH and FDA regulations, along with experience in managing secure genomic and clinical data handling, is essential.

Highest-signal resume keywords

REDCap AdministrationCTDB ConfigurationScripting in PythonData Integration with SQLKnowledge of NIH Regulations

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

REDCap AdministrationCTDB ConfigurationScripting in PythonScripting in RData Integration with SQLTechnical DocumentationUser SupportSystem ValidationBackup ManagementAccess Control

Soft Skills

Collaboration in Multidisciplinary TeamsCommunication with Regulatory Staff

Tools & Technologies

Clinical Research ApplicationsHosting EnvironmentsGenomic Data HandlingClinical Data Transfer

Certifications & Qualifications

Current Human Subjects Protections TrainingGCP Training (CITI or Equivalent)

Industry Keywords

NIH RegulationsFDA RegulationsGood Clinical PracticeFISMANIST 800-53NIST 800-17121 CFR Parts 1121 CFR Parts 5021 CFR Parts 54HIPAA

Tech Stack

Tools & technologies

PythonSQL

About the role

Key responsibilities & impact

Administer, configure, and migrate REDCap, CTDB, and other clinical research applications
Manage approved hosting environments, including backup, access control, and system validation
Support secure handling and transfer of genomic and clinical data
Develop and maintain scripts and data integrations using technologies such as Python, R, and SQL
Produce technical documentation and provide user support
Support NIH or FDA-regulated clinical research programs
Work alongside Government clinical investigators, regulatory staff, and program officials in a multidisciplinary team environment

Requirements

What you’ll need

Bachelor's degree in computer science, bioinformatics, information systems or a related field
Master's degree preferred
Minimum of 5 years of experience supporting clinical research information systems or bioinformatics environments
Administration, configuration and migration of REDCap, CTDB and other clinical research applications
Management of approved hosting environments, including backup, access control and system validation
Knowledge of NIH and federal information security requirements, such as FISMA and NIST 800-53/800-171, as applicable
Support for secure handling and transfer of genomic and clinical data
Scripting and data integration skills (e.g., Python, R, SQL)
Technical documentation and user support experience
Five or more years of direct experience supporting NIH or FDA-regulated clinical research programs
Working knowledge of Good Clinical Practice (ICH E6), 21 CFR Parts 11, 50, 54, 56, 312 and 812 (as applicable), 45 CFR Part 46, and HIPAA
Current human subjects protections and GCP training (e.g., CITI or equivalent)
Experience working in a multidisciplinary team environment alongside Government clinical investigators, regulatory staff and program officials

Benefits

Comp & perks

Competitive rate
Benefit options