.Clinical Data Lead for Mexico City - Office with Flex (3 days at office, 2 days at home)ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.JR125001Clinical Data LeadMexico City - Office with Flex (3 Days at Office, and 2 Days at Home)ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.We are currently seeking a Clinical Data Lead to join our diverse and dynamic team. As a Clinical Data Lead at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.What you will be doingLead and oversee the planning, execution, and delivery of clinical data management activities for assigned projects.Collaborate with cross-functional teams to develop data management plans and ensure adherence to regulatory requirements and industry standards.Provide leadership and guidance to data management team members throughout the lifecycle of clinical trials.Perform data review and reconciliation activities to ensure accuracy, completeness, and consistency of clinical data.Contribute to the development and implementation of data management processes and best practices to optimize efficiency and quality.Your profileBachelor's degree or higher in a relevant scientific discipline.Minimum of 4-5 years of experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry.Proficiency in CDISC standards, FDA/EMA regulations, and ICH-GCP guidelines.Strong technical skills with experience in EDC systems and data management tools (e.G., Rave, Inform, Medidata).Excellent communication, leadership, and problem-solving skills with the ability to work effectively in a team environment and manage multiple priorities simultaneously.Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development