Lead programming support within multiple studies/projects in various study activities to ensures timely and high-quality programming deliverables in assigned projects and areas. Develop and maintain programming documentations and specifications following programming standards and processes Demonstrate company values by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability Understand the scope of work, plan and complete the deliveries and timelines with the study team, programming lead and management Support global regulatory authority submissions including preparing programming deliverable for submission and working closely with partnering functions to address health authority requests. Participate and contribute towards department goals and SME Topics Mentor and Coach new hires and junior programmers.
Required Skills
- Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. Knowledge of other programming languages such as R, Python etc. is a plus.
- Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles). Knowledge of regulatory submissions and requirements is a plus
- Ability to work on global interdisciplinary teams. Good organizational, interpersonal, and communication skills. Positive attitude, team player and growth mindset
- Problem solving and innovative skills that demonstrate initiative and motivation
