Clinical Trial Safety Scientist
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Clinical Trial Safety Scientist at AstraZeneca! Life Sciences Apply Now

Scientist, Clinical Trial Safety

Locations: India – Bangalore

Time type: Full time

Posted on: Posted Today

Job Requisition ID: R-205273

Job Title: Scientist, Clinical Trial Safety

Career Level – C

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.

Essential Skills/Experience:

  • 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

Date Posted: 23-Jul-2024

Closing Date: 27-Jul-2024

APPLY ONLINE HERE

Keywords: Scientist, Clinical Trial Safety job, AstraZeneca, Clinical data review, Patient safety, ICH/GCP Guidelines, SAE reporting, Pharmacovigilance, Clinical studies, Drug development, Full-time job, India, Bangalore. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like TwitterTelegramFacebook and Instagram.

Shekhar
Shekhar Suman is the Co-founder of BioTecNika Info Labs Pvt. Ltd. He is an Entrepreneur, Writer, Public Speaker, and a Motivational Coach. In his career, he has mentored more than 100,000+ students toward success in the Biopharma Industry. He heads the BioTecNika Group, which comprises BioTecNika.com, BioTecNika.org, and Rasayanika.com. An avid reader and listener who is passionate about BioSciences. Today Biotecnika is India's largest Biotech Career portal, with over 5 Million subscribers from academia & Industry. It's ranked among the top 50 websites worldwide in the Biology category.