Senior Principal Clinical Programmer

Role Overview: As a Senior Principal Clinical Programmer at Syneos Health, you will serve as the lead Clinical Programmer, managing and supporting all functional tasks and project deliverables from single study assignments to large programs of studies. You will demonstrate a high degree of independence, technical skills, and the ability to influence the team and clients to achieve results with minimal to no supervision. Your role will involve managing multiple project timelines, leading less experienced programmers, determining the overall strategy for clinical programming tasks, identifying trends across projects, and taking appropriate action to replicate positive results and mitigate negative ones. Key Responsibilities: - Provide clinical programming technical support and expertise across the DM/Clinical Programming function and other departments as needed. - Offer application administration and technical support as the subject matter expert on all core business packages, including but not limited to: Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and supplemental packages such as migration mentoring/review, reporting tools, custom functions, etc. - Utilize primary development tools and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures. - Generate and maintain all required documentation including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding setup, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports. - Monitor applications proactively for workflow alerts, system errors, performance issues, and troubleshoot programming deliverable defects. - Perform system integration activities, application updates, and user acceptance testing. - Serve on project teams to coordinate and lead development activities for clinical programming projects. Attend meetings, participate in discussions, use an analytical approach to problem-solving, focus on deliverables, and provide constructive feedback. - Keep those responsible for project management informed of any issues that might impact project target dates, scope, or budget and escalate potential problems effectively and in a timely manner. - Balance multiple task assignments and communicate needs to supervisor to obtain needed resources. Qualifications Required: - Bachelor's degree in a related field or equivalent work experience. - Minimum of 8 years of relevant experience in clinical programming. - Proficiency in programming languages and tools such as Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, etc. - Strong communication, organizational, and problem-solving skills. - Ability to work independently and as part of a team, demonstrating leadership qualities when required. (Note: Additional details about the company were not provided in the job description.) Role Overview: As a Senior Principal Clinical Programmer at Syneos Health, you will serve as the lead Clinical Programmer, managing and supporting all functional tasks and project deliverables from single study assignments to large programs of studies. You will demonstrate a high degree of independence, technical skills, and the ability to influence the team and clients to achieve results with minimal to no supervision. Your role will involve managing multiple project timelines, leading less experienced programmers, determining the overall strategy for clinical programming tasks, identifying trends across projects, and taking appropriate action to replicate positive results and mitigate negative ones. Key Responsibilities: - Provide clinical programming technical support and expertise across the DM/Clinical Programming function and other departments as needed. - Offer application administration and technical support as the subject matter expert on all core business packages, including but not limited to: Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and supplemental packages such as migration mentoring/review, reporting tools, custom functions, etc. - Utilize primary development tools and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures. - Generate and maintain all required documentation including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding setup, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports. - Monitor applications proactively for workflow alerts, system errors, performance issues, and troubleshoot programming deliverable defects. - Perform system integration activities, application updates, and user acceptance testing. - Serve on project teams to c