Clinical Database Developer I

Job title - Job Title: Clinical Database Developer I

Career Level - C

Introduction to Role:
Join our Oncology R&D team as a Clinical Database Developer I, where you will create the Clinical Database Development (CDD) deliverables on assigned clinical studies. You will be responsible for the quality of CDD deliverables following standards, Standard Operating Procedures (SOPs) and Guidelines. You will also maintain Business Continuity for CDD processes and standards including integrity of the clinical database for the relevant studies.

Accountabilities:
As a Clinical Database Developer, you will be responsible for the timely and quality creation of electronic Case Report Forms (eCRFs), data entry screens, and the design, build and testing of clinical databases. You will also program field derivations, edit checks, consistency checks, validations, procedures and rules. Additionally, you will develop study reporting and visualization environment, create study level documentation for all databases used in data management, and ensure timely and quality system testing and Quality Control (QC) of specified deliverables.

Essential Skills/Experience:
- Bachelor's degree, preferably in computing or scientific discipline
- Database development experience in the pharmaceutical industry working with clinical trial data
- Experience in Study Build activities (Study Design & Validation Rule development) in Medidata Rave
- Basic knowledge of Postproduction changes in Medidata Rave
- Practical experience with object-oriented programming using .NET technologies, C#, Visual Basic, MS SQL
- Excellent written and verbal communication skills
- Ability to work in a global team environment
- Good analytical skills and high attention to detail
- Experience in other EDC tools(Inform, Veeva…etc) are added advantages

- Knowledge of clinical and pharmaceutical drug development process and Clinical trials
- Understanding of data standards (CDISC) and practices 
- Demonstrates professionalism, diplomacy, mutual respect and the ability to manage/value diversity and cultural differences 
- Experience in Medidata Rave Custom Functions 
- Experience with programming languages SAS, Python, R, PLSQL or Java are added advantage

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 are dedicated to following the science. As part of our Oncology R&D team, you will be at the heart of an organization that is committed to pushing the boundaries of science to change the practice of medicine and transform the lives of patients living with cancer. We are a science-based, leading and decisive Oncology enterprise united in our vision to eliminate cancer as a cause of death. With one of the broadest and deepest Oncology pipelines in the industry, there are many opportunities to work with new and novel drugs and help discover what's next.

Ready to join a team that's pioneering bold moves to transform the way cancer is treated? Apply now!

Date Posted

Closing Date

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.