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Tier-1 employer and metro location balanced by niche clinical data requirements, moderate applicant density.
Clinical trial data management is industry-specific, requiring pharma/biotech clinical experience.
Explicit high minimum experience and mandatory clinical data management skills enforce strict shortlisting.
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Accountable for end-to-end management and oversight of study/program clinical trial data to ensure high-quality, timely, decision-ready outputs.
Lead development and execution of Data Management Plan and Integrated Data Review Plan aligned with clinical protocol and program strategy.
Drive database build, UAT, go-live readiness, and oversee study conduct activities including data cleaning, query management, reconciliation, and database lock preparation.
Educational requirement varies from Doctorate to High School diploma with corresponding experience from 2 to 10 years in life sciences, computer science, or business administration.
Work Experience Required: Minimum 2 years (Master’s degree) or 4 years (Bachelor’s degree) or more in relevant fields; 5 years preferred with 3 years in biopharmaceutical clinical research.
Experience working on clinical trials in biotech, pharmaceutical, or CRO companies required.
Experience managing or overseeing external vendors such as CROs, central labs, or imaging vendors is required.
Demonstrated ability to lead cross-functional global clinical trial data management efforts with multiple geographies involved.
Experience managing study-level data quality, delivery metrics, and issue resolution for clinical trial data.
Proven track record in coordinating database readiness, data cleaning, query management, and vendor oversight in a clinical research environment.