Katalyst CRO
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Manager Statistical Programming
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Katalyst CRO . The job was posted 6 months ago. Get AI-powered advice on this job and more exclusive features. Responsibilities
Lead programming support within multiple studies/projects to ensure timely and high-quality deliverables. Coordinate programming documentation and specifications following standards and processes. Demonstrate company values such as excellence, collaboration, innovation, respect, ownership, and accountability. Understand the scope of work, plan, and complete deliveries within timelines. Act as a technical resource for complex programming tasks and standards. Support global regulatory submissions by preparing programming deliverables and working with related functions. Contribute to department goals and SME topics. Requirements
Bachelor's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field with 8+ years of programming experience, preferably in clinical trial data processing. Proficiency in SAS programming with knowledge of R, Python, etc., is a plus. Understanding of pharmaceutical clinical development and regulatory submission requirements. Ability to work with global interdisciplinary teams. Strong organizational, interpersonal, communication, and leadership skills. Experience in managing multiple tasks and projects. Problem-solving skills and the ability to mentor junior programmers. Additional Details
Seniority level: Mid-Senior level Employment type: Contract Job function: Design, Art/Creative, and IT Industry: Pharmaceutical Manufacturing This job posting is currently active. Referrals can increase your chances of interviewing by 2x.
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Manager Statistical Programming
role at
Katalyst CRO . The job was posted 6 months ago. Get AI-powered advice on this job and more exclusive features. Responsibilities
Lead programming support within multiple studies/projects to ensure timely and high-quality deliverables. Coordinate programming documentation and specifications following standards and processes. Demonstrate company values such as excellence, collaboration, innovation, respect, ownership, and accountability. Understand the scope of work, plan, and complete deliveries within timelines. Act as a technical resource for complex programming tasks and standards. Support global regulatory submissions by preparing programming deliverables and working with related functions. Contribute to department goals and SME topics. Requirements
Bachelor's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field with 8+ years of programming experience, preferably in clinical trial data processing. Proficiency in SAS programming with knowledge of R, Python, etc., is a plus. Understanding of pharmaceutical clinical development and regulatory submission requirements. Ability to work with global interdisciplinary teams. Strong organizational, interpersonal, communication, and leadership skills. Experience in managing multiple tasks and projects. Problem-solving skills and the ability to mentor junior programmers. Additional Details
Seniority level: Mid-Senior level Employment type: Contract Job function: Design, Art/Creative, and IT Industry: Pharmaceutical Manufacturing This job posting is currently active. Referrals can increase your chances of interviewing by 2x.
#J-18808-Ljbffr