Associate Director, Clinical Programmer
About the role:
The Associate Director, Clinical Programming is a subject matter expert within the Programming discipline and is accountable for quality, timely and efficient delivery of project programming tasks and quality information management. This position requires seasoned programming experience and extensive industry knowledge to independently lead implementation of programming activities as well as collaborate with and potentially lead other programmers. May involve collaboration on cross-functional teams with a focus on process improvement initiatives.
Role & Responsibilties:
Provides oversight for the full scope of programming deliveries for outsourced studies with our external partners (i.e. Contract Research Organizations)
Responsible for the high quality of all programming deliverables, holding partners and providers accountable for the quality of their deliverable and/or technical subject matter expert for aspect(s) of the TA, Project, or function
Leads internal technical programming activities for internal projects
Leads or contributes to cross-functional administrative or process improvement initiative(s)
Drives the development of best practices to improve quality, efficiency and/or effectiveness within the function
Drives standards development and implementation
Manages and escalates risk in complicated or novel situations within their study and/or projects
Provides tactical input and/or drives ideas and improvements
Supports recruiting efforts and/or provides training and mentorship
Sees opportunities to improve methodology and provides practical solutions for problems
Influences stakeholders by providing subject matter expertise on programming related items
Ensures compliance to standards and automation usage
Employs best project management practices in managing technical projects
Provides input to capacity management for all projects in scope
Maintains current expertise of relevant industry and regulatory requirements
Requirements:
Degree in a quantitative discipline, i.e., Mathematics, Engineering, Statistics, Computer Science, or equivalent knowledge
Minimum 5 years industry clinical programming experience
Advanced SAS programming skills
Thorough knowledge of the clinical development process
Thorough knowledge of industry standards and ability to implement them
Ability to apply programming expertise to problem solving and troubleshooting for teams
Current knowledge of technical and regulatory requirements relevant for the role
Demonstrated multitasking, planning and organizational skills
Proficient ability to influence relevant stakeholders on programming related items
Ability to manage risk in complicated or novel situations
Stakeholder relations skills
Collaboration skills
Team player mindset
Desirable skills:
Statistical modelling experience
High degree of proficiency in SAS macros
Other programming languages e.g. S-PLUS, R, Python, XML, SQL, etc.
SAS Certification
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AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com.
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