We view our employees as the unequivocal ingredients to success. Each and every employee is an integral member of the Cytokinetics team, contributing to our shared goal of improving lives. While expectations of our employees are high, there is an equal commitment to ensuring that contributions are recognized and rewarded. We seek exceptional individuals to join us in our mission to develop potential medicines to improve the health span of people with cardiovascular and neuromuscular diseases of impaired muscle function.

This role will report to the Sr Director, statistical programming and provides deeply impactful leadership on operational and staffing strategies, processes, and quality and efficiency improvements across the entire Statistical Programming department.

Responsibilities                                                                                            

• Lead statistical programming activities as the product lead for one or multiple compounds to support timely and high-quality assembly, reporting, and submission of data on all clinical studies in assigned product(s)
• Lead process improvement initiatives that facilitate standards, infrastructure, and process enhancements across Biometrics, decide on their designs and implementation, and provide advice as a contributor on other such efforts
• Provide technical leadership and ensures adequate statistical programming support for an indication/disease area
• Assist Statistical Programming head to ensure successful implementation of Statistical Programming strategies and efficient execution of the statistical analyses for an indication/disease area
• Provide in-depth guidance, oversight or hands-on programming on assigned products or similar projects to ensure accuracy, completeness, quality, and timely delivery of statistical programming deliverables supporting clinical trial analysis, reporting, and regulatory or other stakeholder review
• Review, and comment on CRFs, edit checks and other study related documents
• Participate in the review of statistical analysis plans, draft TFL specifications, design analysis data sets, and provide inputs for SDTM mapping
• Participate in vendor qualification/selection and monitor vendor performance. Oversee CRO’s deliverables
• Develop and contribute to company SOPs, work instruction, best practices, and other guidance documents for the entire department and beyond; provide impactful feedback into such documents authored by others
• Keep abreast of literature and advancements in SAS

Qualifications

• Bachelor’s degree in a statistics, computer science, mathematics, or related fields with 12+ years of biopharmaceutical experience as a Statistical Programmer
• 5+ years of supervisory experience
• Extensive knowledge and understanding of SAS® programming concepts and skills
• Strongly demonstrated proactivity and superb attention to detail
• Thorough understanding of and hands-on experience with CDISC SDTM and ADaM standards
• Experience leading integrations (ISE/ISS), regulatory submissions, or similar
• Experience contributing directly to departmental budget and resource planning exercises
• Demonstrated proficiency in communicating and presenting complex ideas to varied audiences
• Strong leadership skills and team work spirit, communicating effectively
• Ability to execute and manage multiple simultaneous projects and deadlines with shifting priorities and resources in a fast-paced working environment

Now is the perfect time for you to consider a move to Cytokinetics where you can put all of your skills to maximum use. You will enjoy a truly unique culture as well as a competitive benefits program.