Analyst Clinical Data Management

Design, develop, validate, and maintain clinical study databases within EDC systems, ensuring data quality, protocol compliance, and timely study deliverables in alignment with regulatory and organizational standards.

Requirements

• Hands-on experience in EDC database programming within clinical trials.
• Experience working on Phase I–IV studies preferred.
• Exposure to database build, testing, and maintenance activities.
• Ability to interpret study protocols and translate them into database specifications.
• Experience in creating edit checks and validation rules.
• Capability to manage multiple tasks within defined timelines.
• Basic understanding of CDISC standards and regulatory compliance (GCP).

Benefits

• Life insurance
• Health insurance
• Disability insurance
• Retirement plan