Responsibilities

Manage all data management activities according to quality standards and regulatory requirements, ensuring adherence to project timelines and goals.

• Oversee the development of CRFs and CCGs with other functional area representatives, ensuring all data management databases are developed and validated.
• Manage interactions and deliverables with third-party vendors and CROs, ensuring proper execution of data management activities and providing relevant metrics to the study team.
• Monitor outsourced data management activities for efficiency and regulatory compliance, providing feedback on vendor selection.

Requirements

• Bachelor's degree or equivalent combination of education.
• 4 years of relevant experience in clinical data management within biotech or pharmaceutical/drug development.
• Preferred experience in vendor management and global operations.

Key Skills:

• Strong planning and project management skills, including risk assessment and contingency planning.
• Effective communication and interpersonal skills.
• Excellent organizational and problem-solving skills with attention to detail.