Clinical Data Management

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Skills Required

Must-Have

Good to Have

Roles & Responsibilities

• Manage clinical trial data from EDC systems such as Veeva and Rave.
• Ensure accurate and timely submission of clinical trial reports to regulatory authorities.
• Collaborate with cross-functional teams to resolve issues related to clinical trial data management.
• Maintain compliance with industry standards and regulations in the management of clinical trial data.

Job Requirements

• 2–6 years of experience in clinical data management or a related field.
• Proficiency in using EDC systems such as Veeva and Rave for managing clinical trial data.
• Strong understanding of clinical trials regulations (e.g., GCP) and industry standards (e.g., ICH).
• Experience working on multiple projects simultaneously under tight deadlines.

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