Clinical Database Design Manager at IQVIA

Washington, District of Columbia, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

MedTech, Medical Devices, Diagnostics, Clinical ResearchIndustries

Requirements

Bachelor's Degree in Science/Computer Science/Information Technology or Bachelor in Technology
4-6 years of experience in clinical database programming within a CRO, sponsor, or related clinical research environment
Experience with eCRF design and specifications development
Experience writing, programming, or configuring data validation checks; JavaScript experience preferred
Experience with QC, UAT, and writing and executing test scripts
Hands-on experience with EDC systems; Viedoc experience strongly preferred (bonus but not required)
Proficiency in data importing, API configuration, and integration workflows
Experience with custom report programming (e.g., SAS, R, Python, or other relevant tools); R is a strong bonus
Knowledge of ICH/GCP guidelines, 21 CFR Part 11, clinical trial methodology, and regulatory requirements (FDA, EMA, GDPR)

Responsibilities

Design, build, and maintain clinical trial databases in compliance with study protocols and regulatory standards
Develop and optimize custom reports, listings, and dashboards using various reporting tools
Manage data imports from external sources (e.g., labs, imaging systems) and ensure data integrity
Configure and support API integrations to streamline data transfers between EDC systems and other platforms
Collaborate with Data Managers, Biostatisticians, and Clinical Operations to ensure database functionality supports study needs
Provide technical support for database testing, validation, and UAT activities
Maintain clear documentation of programming specifications, workflows, and processes
Troubleshoot and resolve database issues in a timely manner

Skills

Key technologies and capabilities for this role

clinical databasesEDC systemsAPI integrationsdata importscustom reportsdashboardsdata integrityUATdatabase testingprogramming specificationsSQLregulatory compliance

Questions & Answers

Common questions about this position

What experience level is required for the Clinical Database Design Manager role?

The role requires 4-6 years of experience in clinical database programming within a CRO, sponsor, or related clinical research environment.

What technical skills are essential for this position?

Key skills include experience with eCRF design, data validation checks (JavaScript preferred), EDC systems (Viedoc strongly preferred), data importing, API configuration, and custom report programming with tools like SAS, R, or Python.

What is the required education for this job?

A Bachelor's Degree in Science, Computer Science, Information Technology, or Bachelor in Technology is required.

Is this a remote position or does it require office work?

This information is not specified in the job description.

What is the salary or compensation for this role?

This information is not specified in the job description.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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