Clinical Data Standards Specialist

About the position
Digital Health, the point at which healthcare, technology, data and analytics converge is an area of great promise with the potential to improve the health of everyone. The Drug Development Data platform team within AstraZeneca has the goal of improving patient experience and outcomes and shortening the time it takes to bring life-changing medicines to patients.

You will be joining R&D IT - an outstanding organization at the forefront of the technology revolution in healthcare. It provides the technology, engineering, data and analytics expertise which delivers the Data Platform underpinning AstraZeneca’s Digital Health strategy and R&D transformation programs. The ambition for this Platform is huge. We are looking for data, technology and change experts to work with R&D IT that will ensure this ambition is met.

Main focus for this assignment is on our CDSIC standard development. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards, and praxis.


Responsibilities
Main focus for this assignment is on our CDSIC standard development. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards, and praxis.



Your profile
- Minimum educational level is a BSc degree in a relevant subject such as statistics, biostatistics, mathematics, computer science, life science or engineering
- Expertise in clinical data standards development, in CDISC and standards development within Pharma industry
- Good collaboration, communication and influencing skills
- Good written and spoken English

Personal Qualities Candidates should possess good social skills, be strong team player and be able to work effectively in a global organization where teams often are geographically dispersed. You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude. It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them. Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical development.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

It suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.