MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from concept to commercialization, offering expertise in regulatory strategy, clinical trial design and execution, market access, and post-market optimization. Our teams combine deep therapeutic knowledge with advanced data and technology to help clients make smarter decisions and thrive in the market. Join our team to help shape the future of MedTech.
Position OverviewMCRA, 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 ResponsibilitiesDesign, build, and maintain clinical trial databases in compliance with study protocols and regulatory standardsDevelop and optimize custom reports, listings, and dashboards using various reporting toolsManage data imports from external sources (e.g., labs, imaging systems) and ensure data integrityConfigure and support API integrations to streamline data transfers between EDC systems and other platformsCollaborate with Data Managers, Biostatisticians, and Clinical Operations to ensure database functionality supports study needsProvide technical support for database testing, validation, and UAT activitiesMaintain clear documentation of programming specifications, workflows, and processesTroubleshoot and resolve database issues in a timely manner
QualificationsBachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology4-6 years of experience in clinical database programming within a CRO, sponsor, or related clinical research environmentExperience with eCRF design and specifications developmentExperience writing, programming, or configuring data validation checks; javascript experience preferredExperience with QC, UAT, and writing and executing test scriptsHands-on experience with EDC systems; Viedoc experience strongly preferred (bonus but not required)Proficiency in data importing, API configuration, and integration workflowsExperience with custom report programming (e.g., SAS, R, Python, or other relevant tools); R is a strong bonusKnowledge 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
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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.