Associate Director, Clinical Data Management

Role: Associate Director, Clinical Data Management at a biopharma company focused on innovative drug discovery platforms. Responsibilities: lead strategic planning and operational oversight of clinical data management, ensuring data integrity, quality, compliance, and regulatory adherence; design and maintain electronic data capture systems; collaborate with cross-functional teams including biostatistics, clinical operations, and regulatory affairs; mentor team members and address complex data challenges. Requirements: postgraduate degree with 8+ years (or Bachelor’s with 10+ years) in Life Sciences, Biostatistics, or Computer Science; extensive clinical data management expertise; proficiency in EDC systems like Veeva; in-depth knowledge of industry and regulatory standards; leadership and analytical skills; oncology experience preferred. HighValue: clinical research, data management, oncology, EDC tools, regulatory compliance, cross-functional collaboration. WorkSetup: hybrid onsite (Jersey City or Millbrae), minimum 3 days/week onsite.