Associate Director Statistical Programming Jobs in Arlington, MA

Are you an experiencedManager and Leader inStatistical Programmingwitha deepknowledge of clinical drug developmentand line management experience? Would you like to be part of a fast-paced and agile global team that hasa directstrategic impact on drug development, empowered and trusted to innovate and experiment? Join us at AstraZenecaOncologyBiometrics toimpacta wide range of engaging projects striving to make a difference for millions of patients. Our Biometrics team consists of Statisticians,Programmersand Information Scientists. We drive and contribute tooptimizedclinical drug development programs and access to information and scientific knowledge management.

We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role asStatistical Programming Director,providing strategic programming leadershipand line managementwithinOncBiometrics and collaborating with global product development teams.

Accountabilities:

This position will work in the Early Oncology Programming group and will be accountable for a large and diverse portfolio of products that cover phase 1 / 2 trials in various mechanisms of action and covering multiple indications within oncology.You willbe responsible formanaging and mentoring a group of programmerswho are in turnaccountable forefficientdelivery onstudiesthat are both outsourced and delivered internally,ensuring high-quality of deliverableswhilecomplying withAZ andindustry standards,SOPsandGxPrequirements.Youwillalsobe part of the larger programming leadership team within oncology programming, andresponsible for various activitiesbeyond clinical trials, such asproving strategic or SMEcontributions oncross-functional teams to deliver continuous improvement, innovation, and automation solutions.

Essential Skills/Experience:

• Minimumbachelor's degree in mathematics(e.g.,Applied Math, Engineering,etc), Statistics, Computer Science, Life Science, PublicHealthor equivalent experience

• Minimum10years of experience with advanced knowledge of the clinical development process and industry standards

• 7+ years people and or project management experience

• Advanced SAS programming skills in a clinical and statistical data environment

• Demonstrated programming leadership capability with ability to develop teams and individuals and lead them towards a common goal

• Demonstrated influencing,planningand organizational skills

• Ability to provide input to functional strategies

• Strong project management skills and experience with scope management, resource management,financial management, projectplanningand resource allocation

• Significant experienceinleadershipcapacity with a focus onidentifying,leading,and advancing talent.

• Experience working in a clinical development organization with a heavy emphasis on support of multiple, ongoing projects

• Thorough understanding of pharmaceutical clinical development (i.e.understanding of statistical concepts, techniques, and clinical trial principles) and ability to manage and lead regulatory submissions.

• Thorough understanding of industry standards such as CDISC and 21CFR Part 11.

• Strong ability to solve problems, recommend process improvements, andexecuteprocess improvements.

• Ability to lead and influence teams

• Excellent verbal and written communication skills in a global environment.

• Proven ability to work with cross functional teams, specifically Data Management, Biostatistics, Epidemiology, Clinical Operations, and Pharmacovigilance toinitiate, lead and execute new initiatives and process improvements.

• Recognize behaviors that align with our values critical to the success of our employees, mission, and businessobjectives.

Desirable Skills/Experience:

• Broad experience, ideally across multiple therapeutic areas and outside of the field of Statistical Programming

• Previousoncology experience, ideallyin bothhemeand solid tumor

• Knowledge / experience using open sourceand/or AIin Statistical Programming

• Experience in regulatory submissions and interactions

• Demonstrated experience designing and implementing business processes

• Willingness and ability to travel

The annual base pay (or hourly rate of compensation) for this position rangesfrom $168,830.40 - $253,245.60 USD. Ourpositions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coveragein accordance withthe terms of the applicable plans.

AstraZenecais 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 emailingAZCHumanResources@astrazeneca.com(opens in new window).

WhyAstraZeneca:Here, ambitious science meets real-world impact. You will work in an environment that pairscutting-edgeplatforms-multi-omics, single-cell and spatial technologies, AI/ML, and advanced imaging-with a pipeline that moves decisively from discovery to the clinic. We bring diverse specialists together to ask bold questions, pressure-test ideas, and accelerate progress against some of the hardest-to-treat cancers, valuing kindness alongside ambition so you can stretch your skills while making a tangible difference for patients.