Clinical Research Systems – Bioinformatics Specialist

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🔥 0 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 13%

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Saratoga Ascend

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 1985

🏥 Healthcare

🎯 Recruiter

🏛️ Government

Healthcare • Recruitment • Government

Saratoga Ascend is a federal- and state-focused healthcare workforce and solutions firm that connects cleared, credentialed healthcare professionals with government, military, and civilian healthcare facilities across the U. S. The company provides clinical and non-clinical staffing, clinical lab and scientific staffing, call center services, federal healthcare consulting, IT solutions, program and administrative support, and SLED (state, local, education) services. With a stated four-decade legacy, nationwide coverage, rapid-fill capabilities, strict credentialing/compliance processes, and operation under federal contract vehicles, Saratoga Ascend positions itself as a government-focused healthcare staffing and program management partner.

📋 Description

• 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

• 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

• Competitive rate • Benefit options

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