Associate Director, Clinical Scientist

Responsibilities:

• Lead clinical data review to support data quality, interpretation, and patient safety.
• Identify and escalate clinically relevant findings and resolve data-related issues with study teams.
• Contribute to clinical documents including protocols, investigator brochures, and regulatory materials.

Collaboration:

• Partner with Medical Directors and cross-functional study teams across Clinical Operations, Data Management, Biostatistics, and Regulatory.
• Prepare and present clinical data and scientific information for investigator meetings, advisory boards, and study committees.

Qualifications:

• PhD or equivalent with 2+ years of relevant experience, or bachelor's/master's with 5+ years of post-graduate pharmaceutical experience.
• Hands-on experience reviewing, analyzing, and interpreting clinical trial data.
• Oncology, neurology, or rare disease experience preferred.