AstraZeneca Hiring Clinical Trial Safety Scientist

AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.

Post : Scientist, Clinical Trial Safety

Job Description
Introduction to Role:
Join our dynamic team at the Trial Safety Review Center (TRISARC) in the Research and Development function of AstraZeneca. As a Scientist, Clinical Trial Safety, you will play a pivotal role in reviewing large amounts of clinical data to ensure patient data is complete and medically accurate. This role offers an exciting opportunity to work closely with Senior Scientists, Senior Analysts and Associate Director, Scientists Clinical Trial Safety, supporting them in reviewing important medical data in clinical trials.
Accountabilities
In this role, you will support the team during study start-up activities, review patient-level clinical/safety data on an ongoing basis, schedule and facilitate different types of meetings, and create visualizations from applicable tools. You will also be responsible for performing quality checks of documents, updating study statuses in trackers, and ensuring TRISARC platforms contain up-to-date information.

Candidate Profile
• Educational degree (BSc/Msc/PhD) in Life Science or equivalent work experience in directly related fields
• Knowledge of ICH/GCP Guidelines
• Knowledge of SAE reporting requirements
• Strong attention-to-detail and analytical skills
• Ability to multi-task in a high-volume environment with shifting priorities
• Excellent time management
• Team player, able to work individually
• Computer proficiency
• Excellent knowledge of spoken and written English
• Pharmacovigilance background or experience working on clinical studies
• Clinical/medical background and practical experience providing a stable good knowledge base for reviewing SAEs and other safety events
• Understanding of the clinical study and drug development process
• Programming experience

Additional Information
Job ID : R-205274
Qualification : BSc / Msc/ PhD in Life Science
Location : Bangalore
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Trial Safety
End Date : 27-Jul-2024