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.

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.

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.

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
• Manage each of the data management projects to which assigned; provide leadership to the corresponding data management teams.
• Represent WCT in all dealings with Sponsors with respect to the Data Management aspects of the projects to which assigned.
• Liaise with the Director, Data Management at regular intervals to discuss progress and any issues outstanding.
• Take responsibility for staff training for all projects to which assigned; both direct involvement in training and supervision of staff assigned to training.
• Ensure that all data management operations are conducted to WCT SOPs; contribute to the ongoing revision/improvement of these SOPs.
• Create and review project specific documentation for assigned trials, i.e. the Data Management Plan and the Data Management File.
• To ensure that adequate QC checks (including spot checks) and Database Quality Assessments on the clinical databases of assigned projects.

What you will bring to the role

• Strong knowledge of data management best practices & technologies as applied to clinical trials.
• Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams.
• Strong understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
• Strong analytical and problem solving skills.
• Independent and autonomous project oversight skills.
• Excellent attention to detail. Excellent written and verbal communication skills.

Your experience

• Educated to degree level (preferably Life Science), Nursing qualification, or relevant industry experience
• Min of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.

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.