Statistical Programming - Intern

As a Statistical Programming Intern, your role involves providing robust statistical programming support for multiple clinical projects using SAS to deliver key regulatory-compliant outputs. You will be responsible for developing programming documentation, writing efficient code, and staying updated on statistical programming techniques. Your duties also include providing study updates to the study lead while performing your assigned tasks. - Provide statistical programming support for multiple clinical research study projects or study teams under the oversight of the lead programmer. - Support key deliverables based on regulatory requirements for clinical research e-submissions and/or study requirements for Sponsor, Regulatory, Investigator, or Safety review meetings. - Assist in the development of programming documentation and annotations, including specifications, adhering to relevant Standard Operating Procedures. - Ensure accurate, effective, and timely communication of issues and status to the study lead of the team. - Execute assigned tasks with high quality and integrity. - Work effectively and collaboratively with cross-functional teams. Qualifications Required: - Bachelor's or master's degree in science with 0-6 months of Statistical programming experience in CDISC/TLF. - Familiarity with SAS (mandatory) and R (Optional). - Ability to prioritize, problem-solve, organize, and make decisions. - Good communication skills. - Attention to detail. - Excellent analytical and problem-solving skills. If there are any additional details about the company in the job description, please provide that information.,