Multiple Locations: Nottingham, UK • Tbilisi, Georgia • Warsaw, Poland • Zagreb, Croatia • Bucharest, Romania • Belgrade, Serbia • Metropolitan City of Rome, Italy • Georgia, USA • Italy • Bulgaria • Spain • Czechia • Croatia • Romania • Hungary • United Kingdom • Serbia • Poland
Who we are
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What Global Data Management does at Worldwide
Data Management is an ever growing and collaborative department. Our global team is a group of diverse individuals with wide-ranging experience within the industry. From start to finish, we are involved in clinical studies beginning with building the study database, to locking and delivering the final dataset for the project. Data Management reviews and ensures the clinical study data is of high quality for regulatory submissions.
The Data Management group is the perfect place to launch or further your career. Whether it is technical expertise, or coming from a clinical background, you’re able to hone and expand your skillset within our department. Spanning various roles from data support staff, database and SAS programmers, coders and functional leads, there is place for you!
What you will do
- To co-ordinate and perform processes associated with the configuration, maintenance and validation of databases and database systems and associated applications.
- To review specifications for the set-up and modification of project specific data entry software (including edit check specifications) Review validation plan for edit check and reconciliation check specifications.
- Develop, test, and run SAS programs for clinical data management. This includes programs for data validation and reconciliation checks, data listings and data transfers.
- To configure database/eDC software (both internal and 3rd party) for the use of DM, sponsor and sites. To perform testing of databases and related applications according to IT and Data Management departmental SOPs, both for initial set-up and maintenance.
What you will bring to the role
- Be able to demonstrate good written and verbal communication skills.
- Be able to demonstrate a methodical and logical approach to problem solving and the ability to learn new tasks quickly.
- Be able to work with close attention to detail.
- Be questioning about the validity of data being entered/extracted.
- Key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change.
- The job holder must be computer literate and numerate with a willingness to adapt to various computer systems.
Your experience
- Be educated to degree level or relevant experience
- At least 5 years experience of Data Management Systems and Software
- An understanding of CDISC SDTM standards
- Experience of SAS programming language