Clinical Systems Lead - UK/Serbia- Home-Based

Job Title: Clinical Systems Lead

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 almost 3,000 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.

What Clinical Systems does at Worldwide

Clinical Systems Lead  is responsible to Execute the successful implementation of assigned clinical system projects by ensuring high quality execution and work products and by meeting the established project budget and schedule

• Act as the functional lead for delivery of one or more clinical system study implementations by:
• Providing periodic demonstrations of system functionality to internal and client stakeholders, capturing and resolving issues and requests for change
• Perform configuration and study setup to meet study timelines, fulfill business and technical requirements, and align with SOPs
• Ensure live study implementations are functioning to meet their service level agreements by responding to stakeholder communications, analyzing and resolving issues encountered, and implementing bug fixes where required and in alignment with SOPs

What you will bring to the role

• Ability to communicate concisely and effectively in both written and spoken English
• Proficient client-facing skills
• Proficient in the use of common office software
• Able to work independently or in a multi-disciplinary team
• High attention to detail
• Able to be creative, adapt to new technologies, concepts and processes, make improvements and solve problems

Your experience

• Educated to degree level in a relevant discipline or be able to demonstrate equivalent experience
• 2+ years’ experience in a combination of Contract Research Organization (CRO) experience, CTMS or IRT study delivery, or clinical systems configuration desired
• Experience working in regulated environments such as clinical trials (GAMP, ISO Standards)
• Understanding of clinical trials, blinding, patient safety, data integrity and associated regulations

Why Worldwide

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers. 

Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers!