Scientist Job in Clinical Trial Safety- AstraZeneca
If you’re aiming to grow your career with a global leader like AstraZeneca, then this opportunity is designed for you. The Scientist, Clinical Trial Safety position is an ideal scientist job for professionals seeking impactful clinical jobs within a world-class organization. Located in a rapidly expanding biotech hub, this opening is perfect for those searching for high-growth jobs in Bengaluru while exploring long-term prospects through AstraZeneca careers.
Job Details:
- Job Title: Scientist, Clinical Trial Safety
- Location: Bengaluru, Karnataka, India
- Job ID: R-240643
- Global Career Level: C
- Closing Date: 12-Dec-2025
About AstraZeneca
At AstraZeneca, we are driven by our passion for science and innovation. Our commitment to exploring new frontiers in healthcare allows us to tackle some of the world’s most complex diseases. By fusing data and technology with scientific breakthroughs, we aim to make a significant impact on patients’ lives globally. Our inclusive environment encourages collaboration across diverse teams, fostering an atmosphere where curiosity thrives. With opportunities for lifelong learning and career development, AstraZeneca is where you can truly make a difference.
Qualifications:
- Medical and dentistry graduates
- Strong understanding of ICH/GCP Guidelines
- Experience with SAE reporting
- Analytical skills and strong attention to detail
- Ability to handle high-volume workflows and shifting priorities
- Excellent time management
- Independent and collaborative work capability
- Computer proficiency
- Excellent English communication
Scientist Job Description:
The Scientist, Clinical Trial Safety role sits within the Trial Safety Review Center (TRISARC) at AstraZeneca, supporting critical clinical trial operations that ensure the accuracy and safety of patient data. This role is essential for those seeking high-impact clinical jobs within a global research environment.
Key Responsibilities for Scientist Job:
- Generating and managing documents during study start-up according to applicable procedures and best practices
- Reviewing patient-level clinical/safety data for accuracy, completeness, and coding consistency
- Raising queries as needed for clear medical assessment and case closure
- Scheduling and facilitating meetings
- Creating visualizations, preparing slides, reports, and safety data summaries
- Performing quality checks and filing TRISARC documents in eTMF
Other Responsibilities:
- Handling tasks assigned by the PTS/TRISARC LT
- Contributing to non-drug project work and process improvements
- Updating study statuses per therapeutic area on request
- Ensuring TRISARC platforms (SharePoint) are updated and coordinated
- Monitoring TRISARC mailboxes
- Participating in study meetings such as SSPR
- Maintaining TRISARC distribution list
Desirable Skills:
- Background in Pharmacovigilance or clinical studies
- Experience reviewing SAEs and safety events
- Understanding of clinical development processes
- Knowledge of clinical data flow
- Programming experience
