Ndeye Seck

Background

About Ndeye Seck

With about 10 years of experience in clinical research, I’ve managed +30 clinical trials and investigations in nutrition-metabolic disorders, neurological diseases (MD), oncology, vaccines, malaria, schistosomiasis, and neonatal sepsis across Europe and Africa. My focus is on delivering high-quality projects by ensuring smooth operations, regulatory compliance, and effective teamwork: Strong understanding of clinical trials in Europe & Africa, with experience managing the challenges of different regulatory environments and logistics: I manage all regulatory aspects of clinical trials, ensuring projects run smoothly and meet compliance standards: I’m known for building and leading strong teams. I provide training that boosts team readiness, consistently meeting sponsor expectations, I’ve worked with pharmaceutical companies, NGOs, and CROs in EU and sub-Saharian Africa (east, West and South Africa). My approach combines global best practices with a deep understanding of local needs, helping to strengthen clinical research in underrepresented regions. ’? I’m looking to grow my influence in regulatory affairs and clinical research. I’m excited to connect with professionals who share my passion for making a difference in global health. Let’s explore how we can work together!