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Tier-1 brand and metro location increase applicants, but clinical trial niche moderates overall competition to medium.
Role requires EDC and clinical trial data management experience, limiting cross-industry transferability.
Explicit mandatory clinical execution years and domain-specific clinical trial experience make shortlisting strict.
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Execute core clinical trial data management tasks including database build testing, data cleaning, query management, reconciliation, and lock preparation with limited oversight.
Support Data Management roles by owning and delivering time-sensitive, high-quality outputs across the study lifecycle.
Coordinate with internal teams and external partners to ensure aligned delivery and contribute to process improvements and best practices in data management.
Education: Master's degree OR Bachelor's degree plus 2 years clinical execution experience OR Associate's degree plus 6 years clinical execution experience OR High school diploma/GED plus 8 years clinical execution experience.
Work Experience: At least 3 years in life sciences or medically related field, including 1 year biopharmaceutical clinical research experience on global clinical trials in biotech, pharmaceutical, or CRO.
Experience working in Data Management on global clinical trials is mandatory.
Notice Period: Not explicitly mentioned in the JD.
Experienced in delivering operational data management activities in global clinical trial settings, demonstrating ability to manage multiple stakeholders including internal and external teams.
Capable of independently handling time-sensitive deliverables with high quality and contributing to tracking of deliverables, risk identification, and escalation.
Familiar with EDC/non-CRF data structures, coding dictionaries, and data integration relevant to clinical trials within biopharmaceutical contexts.