Senior Standards Developer I

5 months ago

Bangalore, India AstraZeneca Full time

Job Title: Senior Standards Developer I

Career Level - D

Introduction to role:
Join our Biopharmaceuticals R&D team as a Senior Standards Developer I, where you will be responsible for delivering moderate complexity AZ end-to-end Clinical Analysis and Reporting Standards in your area of expertise. This role requires technical skills and adequate industry knowledge to independently perform tasks while using judgement about seeking guidance in complex situations. You will be primarily responsible for the development and creation of study metadata for SDTM and ADaM in a specific system.

Accountabilities :
As a Senior Standards Developer I, you will develop and maintain one or more median/high complexity analysis and reporting standards. You will monitor and update requests within a defined system, perform independent quality control, and lead the quality of your own deliverables. You will also contribute to the development of best practices to develop, maintain and publish data standards consistently. Collaboration with clinical standards governance groups is key, as is contributing as a subject matter expert support to drug projects on AZ Clinical Standards. You will also assist with metric reporting on standards and requests, and contribute to the function by training and mentoring.

Essential Skills/Experience:
- BSc in Information Sciences, Mathematical, Statistical, Computer Science or Life Science or equivalent experience.
- Accomplished in specialised standards development skills or accomplished experience in Biometrics functions.
- Knowledge of MS Excel, deep attention to the details and a systematic approach to work.
- Good knowledge of the clinical development process.
- Good Project management skills.
- Good knowledge of industry standards (eg, CDASH, SDTM, ADaM).
- Good knowledge of the structure and application of clinical dictionaries including MedDRA, WHODrug Global, and Labcodes.
- Good knowledge of medical terminology and pharmacology as it relates to pharmaceutical drug development and associated regulations.
- Good communication skills in both written and spoken English.
- A clear demonstration of behaviours of truth seeking rather than success seeking.
- Embracing peer review.

Desirable
- Ability to apply clinical data standards technical knowledge to problem solving.
- Ability to proactively manage concurrent activities within role.
- Understanding of programming languages (eg, SAS, R, Java, Groovy, Spotfire, C/C++, VBA/VBS, .NET, Python, Pearl).
- Clinical Laboratory experience.

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.

At AstraZeneca, we follow the science unlike anywhere else. We are driven by our desire to understand and reveal new insights. We are free from fear of failure, free to ask the right questions, make bold decisions, and dig deep into the biology of complex disease. We are always listening and learning from people who live with the diseases our medicines treat. It enables us to better understand their needs and, ultimately, diagnose and design the right treatments to impact patients' lives. We are harnessing digital, data science & AI to help us achieve the next wave of breakthroughs. 

Are you ready to join a team that's making a difference? Are you ready to follow the science? Apply now

Date Posted

26-Jun-2024

Closing Date

27-Jun-2024

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