Principal Clinical Data Lead

This is what you will do:

• As a Principal Clinical Data Lead in our Clinical Data Management (CDM) division, you are responsible for independently ensuring the accuracy and timely delivery of clinical data for highly complex studies. You will also lead or contribute to the evolution of new concepts, technologies, and standards. Your role extends beyond technical expertise as you'll serve as a positive role model for peers, fostering both technical and interpersonal skills. Your role involves performing various tasks to guarantee the accuracy, completeness, and compliance of data crucial for publications and regulatory submissions. Your involvement in shaping technical landscapes, business strategies, and healthcare environments through contributions to various initiatives is integral.

You will be responsible for:

• Collaborating with peers across the data management function and throughout the organization to identify, design and deliver appropriate data management solutions.

• Completing data management tasks, providing technical expertise, and overseeing project deliverables from Contract Research Organizations (CROs), Functional Service Providers (FSPs), and vendors on a timely basis. • Innovating data collection methods and ensuring the development and delivery of medicines for our patients using strategic thinking, strong collaboration and communication skills, and an entrepreneurial mindset. • Leading or overseeing study-specific study start-up tasks, including case report form (CRF) design, edit check creation, CRF completion guideline (CCG) creation, and user acceptance testing including leading process improvements and enhancements, as needed. Leading the development and maintenance of the data management plan (DMP).

• Leading data validation tasks for complex studies during maintenance and close-out, focusing on data integrity and quality metrics. • Leading ongoing operational support for all activities during clinical trial conduct, including database migrations, ad-hoc report creation, maintenance of external data transfer documents, import/export agreements and data specifications, and support for database lock, archiving, and clinical coding activities. • Ensuring all quality and compliance activities are complete, including medical coding, report generation, drug supply, other database integrations, and external data activities. • Independently monitoring activities and project status for successful project deliverables according to the timeline while participating in initiatives to streamline data management processes.

You will need to have:
• A bachelor's degree in a scientific discipline or equivalent.
• Experience in clinical data management for 5 or 6+ years or relevant
experience.
• Thorough knowledge of the clinical data management and clinical
development process, including regulatory submissions for various agencies
(FDA, EU, etc.) and knowledge of CDASH, application of FAIR (Findable,
Accessible, Interoperable, Reusable) principles, MedDRA/WHO-DD dictionary
coding and versioning, with exposure to digital technology, and data
visualization technology.
• Highly effective written and verbal communication skills are necessary to
interact with personnel at all levels within and outside the company.
• Strong organizational skills demonstrating the ability to work on multiple
projects simultaneously while independently managing responsibilities with
effective time management and impactful outcomes.
• Ability to independently solve complex, abstract problems in cross-functional
business collaboration and independent projects while demonstrating
proactive drive, sound decision-making, and attention to detail.
• Proficiency with technology associated with current and evolving data
management practices, including electronic data capture and data
aggregation, and with exposure to data visualization/analytics, automated
data bots, machine learning/artificial intelligence-based process
enhancements, etc.
• 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 an
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.

We would prefer for you to have:

• A master's degree in a related science field or equivalent.

• Certification as a Certified Clinical Data Manager (CCDM) from the Society of Clinical Data Management.

• Experience in leading study teams and maintaining oversight of all start-up, conduct and close-out activities for multiple or complex studies, ensuring fit for purpose quality (including oversight of FSPs, Vendors, CROs and Collaborative Groups).

• Experience in leading the collection of clinical trial and/or Real-World Data.

• Good understanding of molecule and disease area strategies, healthcare environments, as well as strong scientific and technical expertise.

Date Posted

09-Apr-2026

Closing Date

23-Apr-2026

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.