Associate Director, Safety Data Architect (Remote)

View full description

Requirements:

• Bachelor’s degree in a healthcare discipline (Life Science, Pharmacy, Nursing, or biomedical disciplines) is required.
• Graduate degree preferred.
• 10 years of experience in clinical research in the pharmaceutical industry.
• Experience with project management on cross-functional projects.
• Knowledge of the drug development process, including clinical trial conduct.
• Experience in areas such as clinical operations management, risk management, and drug safety operations.
• Demonstrated effectiveness in multidisciplinary team environments.

Responsibilities:

• Functions as a driver for data in aggregate to enhance safety presentation.
• Coordinates deliverables and meetings to review aggregate data with PST Leads and physicians.
• Identifies potential safety concerns from trial data using clinical expertise.
• Ensures consistent safety perspective across various reports and protocols.
• Supports contribution of clinical trial data to regulatory responses.
• Promotes best practices and knowledge sharing among team members.