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 secure. 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
SUMMARY: To perform the principal programming role, lead and own continuous improvement in the programming function’s operating systems and provide both technical and project consultancy across the function.
RESPONSIBILITIES:
Tasks may include but are not limited to:
• Lead and take full accountability for multiple complex studies (including submissions, integration projects) directly controlling sponsors expectation and working with Biostatistical Operations leadership team to maintain resource and ensure delivery deadlines met.
• Lead large study teams, ensuring all planned activities delivered to time and quality, whilst maintaining team harmony and motivation.
• Manage and organize competing priorities whilst displaying flexibility for change.