Associate Director, Clinical Data Management

Responsibilities:

• Lead end-to-end Clinical Data Management activities.
• Provide operational leadership for study timelines.
• Oversee key CDM activities including Database build, eCRF design, and Data review.

Qualifications:

• BS/MS in Life Sciences, Computer Science, Data Management.
• 10+ years of experience in Clinical Data Management within biotech or pharmaceutical industries.
• Strong understanding of clinical trial processes and global regulatory requirements.

Skills:

• Strong organizational, problem-solving, and project management skills.
• Excellent communication and cross-functional collaboration skills.
• Ability to prioritize and manage multiple studies.