AstraZeneca
Healthcare
ClinicalDataManagerI
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Clinical Data Manager I at AstraZeneca. Skills: Clinical Data Management, Data Quality. Assist with Study level CDM administrative support. Review documentation”
Industry & Context.
Issue resolution
What They're Looking For.
Must Have
University or college degree in life sciences or related subject, pharmacy, nursing or equivalent relevant degree, Fluent English (oral and written), Attention to detail, Good verbal and written skills, Ability to work flexibly on simultaneous projects, Proactively manage time to meet own deadlines, Interpersonal skills, Proven ability to communicate effectively in a global environment
Nice to Have
Basic understanding of clinical trials methodology, Basic understanding of Clinical Data Management, Basic understanding of GCP, Basic understanding of medical terminology
What You'll Do.
Assist with Study level CDM administrative support
Perform User Access Testing
Reconcile third party data
Provide data to clinical teams
Coordinate instream data review
Coordinate lab data review
Collaborate with Data Management Vendor
Oversight of data quality
Oversight of documentation quality
Support DM Delivery Leads to maintain CDM specified
Support DM Delivery Leads to maintain CDM types
Support DM Delivery Leads to maintain CDM milestone
Support DM Delivery Leads to maintain CDM risks
Support DM Delivery Leads to maintain data transfer
Support DM Delivery Leads in oversight of Trial
Perform quality compliance checks
Support DM Delivery Leads in User Acceptance Testing
Resolve issues related to Clinical Data Management deliverables
Input ideas to help resolve issues
Contribute to continuous improvement
Perform CDM related ad-hoc requests
How You'll Work.
Team & Collaboration
Cross-functional study teams; Global environment
Communication Scope
Verbal skills; Written skills
Full Job Description
## **ntroduction to role:** Are you ready to turn complex clinical data into clear decisions that accelerate medicines to patients? Do you want to grow your craft while contributing to pivotal studies from day one? As a Clinical Data Manager I, you will help deliver high-quality, analysis-ready data that drives critical go/no-go decisions across our global clinical portfolio. You will work alongside experienced Data Management Leads, cross-functional study teams and external partners to ensure every data point is reliable, timely and audit-ready—so our scientists and physicians can focus on what matters most: helping patients sooner. You will learn fast, take ownership of meaningful work, and see how your attention to detail and collaboration skills translate into real-world impact. ## **Accountabilities:** * Assist with Study level CDM administrative support based on the relevant model and DM Vendor. This may include but is not limited to activities related to the study start up, conduct and closeout phases. (i.e., documentation review and/or creation, User Access Testing, query management, data cleaning and reviews, third party data reconciliation in accordance with the project study model, KPIs and timelines.). * Day to day responsibilities may include but are not limited to: \- Study status reporting to the relevant clinical study team members, (e.g., provide data to clinical teams for performing medical and clinical reviews, coordination of instream data review, lab data review, etc.) \- Collaboration with Data Management Vendor regarding upcoming deliverables and milestone achievements (i.e., snapshots, interim, and migrations). \- Oversight of the data quality, documentation quality, and types of these deliverables and milestones. * Support DM Delivery Leads to maintain CDM specified systems and types of deliverables, milestone achievements, risks and mitigations and data transfer agreements, and other study administrative needs. * Support DM Delivery Leads i
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