Clinical Data Manager

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!

Clinical Data Manager does at Worldwide Oversee, lead, manage, and provide technical expertise within the assigned projects to ensure that they are executed in an efficient, accurate, and timely manner to the Sponsor’s satisfaction.

What you will do Provide fully independent and autonomous leadership of data management services (start up, conduct, and close out)​ across multiple complex global projects/programs, including: Ensure appropriate resources are allocated to complete all DM activities on time and within budget.

Prepare DM trial documentation (DMP, DB Specifications, Edit check specifications, CCGs, DTAs). Ensure effective UAT is performed. Write external vendor reconciliation specifications for programming reconciliation outputs (e. g. Serious Adverse Events, IRT, Central Laboratory). ​ O