Associate Director, Clinical Data Management

Role: Associate Director, Clinical Data Management at a biopharma focused on innovative molecular imaging for drug discovery. The position involves strategic leadership and operational oversight of clinical data management activities, ensuring data quality, integrity, and regulatory compliance across studies. Responsibilities include developing data collection strategies, designing and maintaining EDC systems, overseeing data validation and reconciliation, and collaborating with cross-functional teams like biostatistics and clinical research. Requirements: Postgraduate degree with 8+ years or Bachelor's with 10+ years in life sciences, biostatistics, or related fields; extensive clinical data management expertise, including database design and quality assurance; proficiency in data management tools (e.g., Veeva EDC preferred), regulatory guidelines, and industry best practices. Preferred: oncology experience and familiarity with clinical research practices. High-Value: focus on clinical research in biotech/pharma, data integrity, regulatory adherence, and cross-functional collaboration. Work setup: minimum 3 days/week onsite in Jersey City or Millbrae, with some flexibility.