Clinical Trial Safety Scientist Jobs at AstraZeneca, Apply Now!
AstraZeneca is hiring a Senior Scientist 1 – Clinical Trial Safety for its Trial Safety Review Center (TRISARC) in Bengaluru. This role is ideal for professionals with a background in life sciences or medicine who are passionate about patient safety in clinical trials. You will play a critical role in data review, medical accuracy, and safety reporting across global studies. Join an organization that combines science and innovation to deliver life-changing medicines and foster career growth in a collaborative, hybrid work culture.
Job Posting: Senior Scientist 1 – Clinical Trial Safety at AstraZeneca
Location: Bengaluru, Karnataka, India
Job ID: R-230942
Career level: D
Introduction:
At AstraZeneca, we are driven by curiosity and courage, exploring what science can achieve. Our commitment to making a difference fuels our passion for innovation as we fuse data and technology with scientific breakthroughs. We embrace lifelong learning opportunities, empowering our team members to grow their careers while impacting patients’ lives globally. With a diverse pipeline and cutting-edge resources, we are dedicated to delivering life-changing medicines.
Introduction to Role
Are you ready to dive into the world of clinical trial safety and make a real impact? At
AstraZeneca’s Trial Safety Review Center (TRISARC), we are dedicated to ensuring that patient data is complete and medically accurate, enabling study physicians and clinical scientists to interpret medical and safety data efficiently. As a Senior Scientist I in Clinical Trial Safety, you will collaborate closely with core and extended study teams throughout every stage of the clinical trial. From setting up well-defined standards and eCRF modules to reviewing critical clinical/safety data during recruitment and maintenance phases, your role is pivotal in maintaining the integrity of our trials. You’ll also prepare and facilitate meetings related to the review of study-level safety data, supporting study teams by writing patient narratives for qualifying events when applicable. Are you ready to take on this challenge?Accountabilities
- Ensure consistent processes and efficient review of critical clinical/safety data
- Review patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness, coding consistency, and generate applicable queries as needed for appropriate medical assessment and case closure
- Prepare aggregated data visualization and facilitate meetings related to review of safety data on study level as Senior Scientist
- Contribute to study start-up activities according to the applicable process/procedures (e.g., input to the applicable documents, tools set up)
- Serve as a member of the Extended Study Team and report on TRISARC deliverables
Essential Skills/Experience
- Educational degree (BSc/MSc/PhD) in Life Science or equivalent work experience in directly related fields (preferably medicine, pharmacy, veterinary, biotechnology, nurse, dentist)
- Minimum two years of experience working on clinical studies and/or study safety methodology as Senior Scientist
- Understanding of the clinical study and drug development process
- Knowledge of ICH/GCP Guidelines
- Knowledge of SAE reporting requirements
Experience using data review tools such as JReview, JMP Clinical, or Spotfire, EDC is desirable.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Keywords: Senior Scientist, Clinical Trial Safety, AstraZeneca, Bengaluru, Karnataka, India, Job Opening. Clinical Trial Safety Scientist Jobs at AstraZeneca, Apply Now!
