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Mid-level clinical data role in Bangalore at a well-known CRO, attracting many qualified applicants.
Role requires clinical trial and regulatory expertise, making skills less transferable across industries.
Requires clinical data tools, regulatory knowledge, and domain-specific experience, so filters are moderately strict.
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Deliver high-quality clinical data management tasks including planning, coordinating, and risk assessing data review processes using various tools.
Collaborate with trial partners and programmers to ensure data review tools are set up, data integrity is maintained, and deliverables are achieved on time.
Conduct data review, issue identification, and resolution, maintain trial documentation, contribute to dashboards and reporting, and prepare for audits and inspections.
Bachelor's degree in Life Sciences or Healthcare or relevant field.
Intermediate knowledge of clinical data management in pharmaceutical or biotechnology industry.
Familiarity with clinical data management systems such as Medidata or Oracle RDC.
Work Experience Required: Relevant clinical data management experience; exact duration not explicitly mentioned in the JD.
Experienced with risk-based data management approaches and clinical trial data review processes involving multiple stakeholders.
Able to manage large datasets, perform data validation and reconciliation, and create/manage data review documentation and dashboards.
Comfortable working in a fast-paced environment with cross-functional collaboration and compliant with regulatory guidelines (e.g., ICH-GCP).