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Tier-1 employer, metro location, and early-mid experience range increase applicant competition.
Clinical trial, EDC and regulatory expertise limit transferability across industries.
Mandatory degree with 2+ years plus EDC/GCP requirements creates moderate shortlisting rigidity.
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Manage Data Monitoring and Management (DMM) activities for clinical trials, ensuring data quality and completeness as per the Data Management Plan.
Contribute to moderately complex clinical data projects by developing short-term work plans, applying standards, and producing data cleaning reports.
Collaborate with local and global subject matter experts to identify and resolve system and process issues, and document lessons learned to improve cross-study learning.
BA/BS with at least 2 years of experience or MBA/MS with any years of experience.
Demonstrated knowledge of data management processes and principles, including proficiency in web-based data management systems.
Working knowledge of electronic document management systems and familiarity with ICH Good Clinical Practices.
Thorough understanding of clinical study management and regulatory operations processes.
Experience using commercial clinical data management systems and electronic data capture (EDC) products in the pharmaceutical industry.
Ability to leverage data visualization tools and AI technologies (e.g., ChatGPT, Microsoft Copilot) to support problem solving and productivity enhancement.
Proactive collaborator who can build strong relationships with subject matter experts and apply regulatory knowledge to ensure operational excellence.