Worldwide Clinical Trials
Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
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 the Data Management department does at Worldwide
Our Data Management team is an ever-growing and collaborative group of diverse individuals with wide-ranging experience within the industry. From start to finish, we are involved in clinical studies – from crafting the study database to ensuring the pristine delivery of the final dataset. We meticulously ensure data accuracy and integrity, crucial for groundbreaking regulatory submissions. With a variety of roles, from data support staff, database and SAS programmers, coders, and functional leads, there are many opportunities to launch and further your career. Our team embraces an environment that invites input, fosters personal growth, and empowers your professional journey.
What you will do
Assist the Data Manager in all data cleaning activities.
Assist the Data Manager with the preparation of trial documentation.
Perform verification and User Acceptance Testing of configured databases.
Assist the Data Manager with the creation and validation of Manual and SAS checks.
Assist the Data Manager with the reconciliation of data from external sources (e.g. Serious Adverse Events, IVRS, Central Laboratory).
Responsible for the registration of users into the EDC/CTMS system, performing system demonstrations if required.
Assist with the maintenance of procedure logs, coding schemes, input notes and Data Entry Manuals. the arrival and logging of data sheets using in-house software and data entry systems.
Conduct components of Database Quality Assessments on the clinical databases as requested by the Data Manager.
Establish and/or maintain correspondence files with participating centres.
Archiving of trial documentation and (e)CRFs.
What you will bring to the role
The job holder must be computer literate and numerate with a willingness to adapt to various computer systems.
It is essential that the job holder works with close attention to detail and is questioning about the validity of the data being entered and has an ability to phrase data queries in an understandable and impartial manner.
To have the ability to train new staff and to monitor their performance.
Your experience
Educated to degree level (preferably Life Science).
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at ! For more information on Worldwide, visit or connect with us on .
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
Worldwide Clinical Trials
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