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Medium — common entry-level clinical data role in metro with a known CRO, moderate applicant density.
High — clinical data management and medical coding skills are highly specific to pharma/CRO environments.
Medium — master's degree and regulatory/GCP knowledge required but no explicit years or niche certifications.
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Enter and verify clinical trial data from Case Report Forms into databases ensuring accuracy and regulatory compliance.
Perform quality control and support data processing activities including database testing and documentation across multiple projects.
Support user access management for EDC systems and collaborate with cross-functional teams to meet project timelines.
Master’s degree in Life Sciences or related field is mandatory.
Basic knowledge of Clinical Data Management and regulatory standards like ICH guidelines and GCP is required.
Strong analytical skills with high attention to detail and proficiency with Microsoft Excel and Word.
Work Experience Required: Not explicitly mentioned in the JD.
Experience or interest in clinical data management within regulated clinical research environments.
Ability to manage multiple priorities in dynamic settings and maintain quality under deadlines.
Capable of working collaboratively in teams and supporting cross-functional project goals.