IQVIA
Position Overview
MCRA, an IQVIA business is seeking a Clinical Database Design Manager to join our growing Clinical Data Management team. The ideal candidate will bring strong technical expertise in building, maintaining, and optimizing clinical databases to support clinical trials across multiple therapeutic areas within the MedTech space. This role requires a creative solutions-driven, detail-oriented professional who is comfortable working with diverse data sources, performing complex integrations, and collaborating with cross-functional teams to deliver high-quality clinical data solutions.
Key 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
Qualifications
Bachelor's Degree in Science/Computer Science/Information Technology or equivalent
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)
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
https://jobs.iqvia.com/eoe
The potential base pay range for this role, when annualized, is $86,800.00 - $217,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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Key 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
Qualifications
Bachelor's Degree in Science/Computer Science/Information Technology or equivalent
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)
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
https://jobs.iqvia.com/eoe
The potential base pay range for this role, when annualized, is $86,800.00 - $217,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
#J-18808-Ljbffr