When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Introduction to role
As a Principal Clinical Data Scientist, you will be responsible for developing Clinical Data Analytics and Reporting functionalities of increasing complexity and may coordinate the work of other personnel developing standard and/or study-specific functionalities. You will provide guidance to more junior personnel and act as a subject matter expert for selected reporting functionalities. Working closely with Data Management, Medical Review and RBQM leads as well as other Data Scientists, your proactive approach to sharing insights and experiences with colleagues, both within and outside the department, is crucial. Your role involves overseeing various projects and tasks and implementing process improvements to support an integrated cross-functional approach to managing quality in clinical study conduct and reliability of study results to support publications and regulatory submissions.
Accountabilities
- Working independently and taking responsibility for specific deliveries within a study or project.
- Designing, developing, and leading the development of data mapping for DM Data Analytics and Reporting. Tasks can involve gathering requirements, programming, testing, documentation, and coordination of work of other involved personnel.
- Maintenance of data mapping and study-specific reports and analyses to ensure they continue to work in line with requirements; acts as a subject matter expert.
- Demonstrating a strong understanding of broader Clinical dat areview strategy and contributing to it by driving cross-functional innovation/optimization projects.
- Staying informed on the data quality needs of regulatory agencies, collaborators, clients, and team members.
- Providing Clinical Data Scientists with guidance on the design and development of data mapping and reporting functionalities.
- Leading activities related to the development of Data Analytics and Reporting for a study or project including overseeing the work of more junior staff, delegating tasks between other engaged team members.
- Identify gaps, lead initiatives, and promote new ways of working, improving standard methodologies with new technologies for enhanced quality management.
- Guide the evolution of data reporting and analytics methodology and processes to deliver medicines by applying critical thinking, collaboration, and communication skills.
- In collaboration with Senior Data Scientist, developing and applying novel analyses.
- Contributing to the function by training and mentoring more junior staff.
- Leading the quality of own deliverables and overseeing the quality of more junior team members.
Essential Skills/Experience
- Educational degree (BSc/MSc/PhD) in Life Science, Computer Science or Information Science and a minimum 5 years of experience in the application of information and knowledge management in a clinical or scientific setting, or equivalent combination of education and experience.
- Good understanding of clinical development, clinical data management, risk-based monitoring, and centralized monitoring methodologies.
- Advanced knowledge of R programming language.
- Excellent communication skills in both written and spoken English.
- Project Management skills.
- Ability to mentor, train, organize, and lead teams.
- Advanced knowledge of SQL,SAS and Spotfire (or other Advanced Analytics Platform(s)).
- The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without accommodation, to use a computer; engage in communications via phone, video, and electronic messaging; engage in problem-solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.
Desirable Skills/Experience
- Minimum of 3 years' experience in the application of information and knowledge management to support Risk-Based Quality Management and/or Centralized Data Review.
- Previous experience with elluminate platform .
- Previous experience with Business Analytics Software, e.g., Power BI / Spotfire / Tableau is an advantage.
- Previous experience with Software Development Lifecycle and computer systems validation.
- Previous experience in life science and clinical studies is an advantage.
- Experience with advanced analytics approaches (e.g., machine learning/AI).
At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the opportunity to be at the forefront of rare disease research and make a meaningful difference in patients' lives.
Ready to lead and inspire? Apply now and take the first step towards a fulfilling career at Alexion, AstraZeneca Rare Disease.
#LI-Hybrid
Date Posted
29-Apr-2025
Closing Date
12-May-2025
Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.