AstraZeneca · 6 hours ago
Analyst, Clinical Trial Safety
US - Durham - NC
Full-time
Hybrid
Entry Level
1+ years expAstraZeneca is a global biopharmaceutical company dedicated to sustainable healthcare solutions. The Analyst, Clinical Trial Safety will support tools set-up, maintenance, and data analysis tasks to ensure the integrity and accuracy of clinical trial safety data.
BiopharmaBiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Supporting Senior Analyst and Associate Director, Analyst in their activities
Data Review tool set-up, maintenance and close-out of study according to agreed Best Practice procedures – to allow for handling of safety data and review for medical completeness and medical accuracy
Generation of high quality reports that are aligned for TRISARC members and the Global Therapeutic Areas
Work with data outputs (i.e., generate reports, macros/scripts) from multiple sources such as the clinical database, external labs, ECG providers, and other safety vendors as appropriate
Generate summary reports
Analyze and visualize clinical data from different sources including but not limited to eCRF, external lab, clinical databases
Tool maintenance and tool improvement; provide customer feedback from the end user (TRISARC Safety Scientists, Study Physicians, Clinical Scientists)
Data analysis and visualization
Input into non-drug project work including training activities, continuous improvement, and development of procedures as needed
Perform quality check of documents and file TRISARC documents in eTMF
Update study statuses in tracker
Ensure TRISARC platforms (e.g., SharePoint) contain up-to-date information, documents, files; coordinate updates, if needed
Support preparation/participate in different type of meetings
Qualification
Required
Bachelor degree in related discipline
1+ years of analytical experience
Analytical skills
Experience in data analysis
Advanced computer skills (Microsoft Outlook, Excel and Microsoft Power Platform)
Proven organizational and analytical skills
Proven ability to prioritize and manage multiple tasks with conflicting deadlines
Ability to work independently, as well as in a team environment
Independently designing and planning own work
Excellent knowledge of spoken and written English
Exhibit of AZ Values and Behaviours
Preferred
Understanding of the clinical study and drug development process
Knowledge of ICH/GCP Guidelines
Knowledge of SAE reporting requirements
Relevant industry or health care experience
Demonstrates ability and willingness to work cross-functionally, on global level
Ability to concisely summarize large amounts of complex information
Programming experience in data analysis and/or data mining set-up (e.g. Python, R, SAS)
Experience using data review tools such as JReview, JMP Clinical, or Spotfire
Statistic knowledge
Company
AstraZeneca
AstraZeneca is a pharmaceutical company that discovers, develops, manufactures, and markets prescription medicines. It is a sub-organization of Investor.
10001+ employees
H1B Sponsorship
AstraZeneca has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2021 (2)
2020 (11)
Funding
Current Stage
Public CompanyTotal Funding
$5.26B2024-07-30Post Ipo Debt· $1.51B
2023-02-28Post Ipo Debt· $2.25B
2023-02-24Post Ipo Debt· $1.5B
Leadership Team
Pascal Soriot
Executive Director and Chief Executive Officer
Aradhana Sarin
Group CFO and Executive Director
Recent News
2026-02-06
Longevity.Technology
2026-02-06
Company data provided by crunchbase