AstraZeneca Clinical Trial Safety Job For BSc, MSc & PhD
AstraZeneca Clinical Data Manager Job For Life Sciences, Apply Online. BSc, MSc & PhD life sciences job opening. Clinical Trial Safety vacancy. AstraZeneca job openings. Interested and eligible applicants can check out all of the details on the same below
Post Name – Scientist Clinical Trial Safety
Location – India – Bangalore
Job ID – R-145282
CAREER LEVEL:
Leverage technology to impact patients and ultimately save lives
Do you have expertise in, and passion for, information technology? Would you like to apply your expertise to impact the IT strategy in a company that follows science and turns ideas into life-changing medicines? If so, AstraZeneca might be the one for you!
About AstraZeneca
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we’re dedicated to being a Great Place to Work.
About Our It Team
It’s a dynamic and results-oriented environment to work in – but that’s why we like it. There are countless opportunities to learn and grow, whether
that’s exploring new technologies in hackathons, or redefining the roles and work of colleagues, forever. Shape your own path, with support all the way. Diverse minds that work cross-functionally and broadly together.About The Role
The Trial Safety Review Center (TRISARC) is a department in the Research and Development function of AstraZeneca. The primary remit of the TRISARC is to review large amounts of safety data flowing through the clinical trial environment in order to ensure patient data is complete and medically accurate thus allowing study physicians and scientists to interpret safety data efficiently.
The Scientist, Clinical Trial Safety will work closely with the Senior Scientists, Senior Analysts and Associate Director, Scientists Clinical Trial Safety to support them in reviewing important and pre-specified medical (mainly safety) data in clinical trials as operated under the Research and Development (R&D) division of AstraZeneca. During the recruitment and maintenance phases of the clinical trial, they use the Center’s data review tools to support review and query important clinical/safety data within the scope agreed with the medical team and documented accordingly. The Scientist also supports the preparation/facilitation of the meetings and management of study documents and trackers relevant to TRISARC activities.
Typical Accountabilities
- Supporting Senior Scientist, Senior Analyst and Associate Director, Scientist in their activities: During study start-up activities by generating/managing the documents according to applicable procedures/standard methodologies, set up/configuration of applicable tools,
- Review of patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness, coding consistency and generating applicable queries as needed to obtain information for appropriate medical assessment and case closure.
- Schedule and facilitate different types of meetings.
- Creating visualizations from applicable tools and preparing slides/reports/data as required.
- Perform quality check of documents and file TRISARC documents in eTMF.
Education, Qualifications, Skills and Experience
- Educational degree (BSc/MSc/PhD) in Life Science or equivalent work experience in directly related fields (preferably medicine, pharmacy, veterinary, biotechnology, nurse, dentist)
- Knowledge of ICH/GCP Guidelines
- Knowledge of SAE reporting requirements
- Strong attention-to-detail, analytical skills, and ability to concisely summarize large amounts of complex information
- Ability to multi-task in a high-volume environment with shifting priorities
- Excellent time management
- Great teammate, able to work individually
- Computer proficiency
- Excellent knowledge of spoken and written English
- An exhibit of AZ Values and Behaviours.
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