ClinChoice is searching for a Principal/Statistical Programmer Analyst/Consultant to join one of our clients.ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the clients counterparts.Main Job Tasks and Responsibilities:The Senior Statistical Programmer Analyst/Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasksKey Responsibilities:Responsible for supporting the Programming deliveries of a clinical study or project.Implements statistical programming aspects of the protocol and the clinical development program.Ensures high quality is built into own deliverables and the quality delivered by other programmers.Programs independently with high efficiency and quality.Writes and/or implements specifications and oversees completeness of relevant documentation.Contribute to the development of best practices to improve quality, efficiency, and effectiveness within the function.Ensures compliance with standards and automation usage.Plans and support team activities and tasks.Communicates and escalates risks within the assigned studies and/or projects.Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader.Education and Experience:Bachelors degree in computer science (CS), statistics, or related scientific disciplines with 6 yrs. of clinical programming (CDISC) experience; Masters degree in CS, statistics or related disciplines with 7 yrs. of clinical programming (CDISC) experience.Need to have Oncology TA experience.Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.Good understanding of the clinical drug development process.Strong communication skills and coordination skills.Current knowledge of technical and regulatory requirements relevant for the roleAbility to proactively manage concurrent activities within a projectProficient ability to influence relevant stakeholders on programming-related items.Please use the below link for job application and quicker response.https://lifelancer.com/jobs/view/e564dcd55e0ce8d95f8482af4d7eb60c