Clinical Data Associate - Serbia - Remote

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 theData ManagementDepartment 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

Toassistthe Data Manager in all data cleaning activities.

Toassistthe Data Manager with the preparation of trial documentation.

To perform verification and User Acceptance Testing of configured databases.

Toassistthe Data Manager with the creation and validation of Manual and SAS checks.

Toassistthe 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 ifrequired.

Toassistwith the maintenance of procedure logs, coding schemes, inputnotesand Data Entry Manuals.

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 isquestioning abou