Job Title: Scientist, Clinical Trial Safety
Company: AstraZeneca
Location: Bengaluru, India
Job Type: Full-time
Summary:
AstraZeneca is seeking a highly motivated and detail-oriented Scientist, Clinical Trial Safety to join our Trial Safety Review Center (TRISARC) in Bengaluru. This is a unique opportunity to contribute to groundbreaking research and development, ensuring the medical accuracy, patient safety, and high quality of clinical data across our innovative programs. If you are a life science graduate or healthcare professional with a passion for clinical trial safety, pharmacovigilance, and patient data review, we encourage you to apply.
About AstraZeneca:
AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines, primarily for the treatment of diseases in three therapy areas – Oncology; Cardiovascular, Renal & Metabolism; and Respiratory & Immunology. Operating in over 100 countries, AstraZeneca’s innovative medicines are used by millions of patients worldwide.
About TRISARC:
The Trial Safety Review Center (TRISARC) is a global initiative dedicated to maintaining the highest standards of medical accuracy, patient safety, and data quality in AstraZeneca’s clinical trials. As a member of TRISARC, you will play a vital role in safeguarding patients and contributing to the development of life-changing medicines.
Key Responsibilities:
As a Scientist, Clinical Trial Safety, your responsibilities will include:
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Supporting Senior Scientists and Analysts:
- Assisting with study start-up activities, including document preparation and tool configuration.
- Reviewing patient-level safety and clinical data for accuracy, completeness, and coding consistency.
- Generating queries to ensure high-quality medical and safety assessments.
- Preparing visualizations, study reports, and presentations to communicate findings effectively.
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Operational & Documentation Support:
- Facilitating and scheduling study meetings, such as Safety Signal Prioritization Review (SSPR) meetings.
- Performing quality checks to maintain the integrity of TRISARC documents in the electronic Trial Master File (eTMF).
- Managing SharePoint platforms and ensuring trackers are up-to-date for efficient information management.
- Overseeing TRISARC mailbox operations and managing distribution lists to ensure effective communication.
- Supporting continuous improvement initiatives to optimize processes and enhance efficiency.
Essential Qualifications:
To be successful in this role, you should possess the following qualifications:
- Bachelor’s (BSc), Master’s (MSc), or Doctorate (PhD) degree in Life Sciences (Medicine, Pharmacy, Veterinary Science, Biotechnology, Nursing, or Dentistry).
- A strong understanding of ICH-GCP (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use – Good Clinical Practice) guidelines and Serious Adverse Event (SAE) reporting requirements.
- Exceptional attention to detail and strong analytical skills for accurate data review and interpretation.
- Excellent English communication skills, both written and verbal, to effectively collaborate with team members and stakeholders.
- Ability to multitask effectively in a high-volume environment, managing priorities and meeting deadlines.
- Strong computer proficiency and teamwork skills to collaborate effectively within a global team.
Desirable Experience:
The following experience is considered an advantage:
- Prior experience in clinical trials or pharmacovigilance.
- Hands-on experience reviewing Serious Adverse Events (SAEs) and other safety events.
- A comprehensive understanding of clinical data flow and the drug development process.
- Basic programming experience.
Why Join AstraZeneca?
- Global R&D Environment: Work in a globally recognized Research and Development environment at the forefront of pharmaceutical innovation.
- Impactful Contributions: Contribute directly to the development of life-changing healthcare innovations that improve patient outcomes.
- Flexible Work Culture: Enjoy a flexible hybrid work culture with a minimum of 3 days onsite in our Bengaluru office.
- Cross-Functional Collaboration: Opportunities to collaborate with cross-functional teams and gain exposure to various aspects of drug development.
- Inclusive and Diverse Culture: Be part of an inclusive, diverse, and people-focused organization where your contributions are valued.
Job Details:
- Role: Scientist, Clinical Trial Safety
- Company: AstraZeneca
- Location: Bengaluru, India
- Job Type: Full-time
- Date Posted: 01-Dec-2025
- Application Deadline: 13-Dec-2025
How to Apply:
Interested candidates are encouraged to apply through the AstraZeneca careers website by the application deadline. We look forward to receiving your application.