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 Central Monitor Department Does At Worldwide
Will conduct central monitoring activities for assigned clinical trials in accordance with ICH GCP E6 requirements
What You Will Do
- Perform central monitoring activities including review of system outputs, identification of outliers, trends or signals and propose actions for assessment by study team. Follow-up with study teams as appropriate for action or issue resolution.
- Ensure the documentation of the centralized monitoring strategy in the appropriate functional plan and/or development of the central monitoring plan
- Conduct and document study/site level review of Key Risk Indications/Key Performance Indicators and where required, statistical monitoring and tracking of study Quality Tolerance Limits
- Ensure Inspection Readiness for centralized monitoring scope.
- Present at Central Monitor Forum meetings
What You Will Bring To The Role
- Excellent Communication skills
- Excellent planning and organizational skills with effective time management
- Knowledge of clinical project financial principles
- Excellent planning and organizational skills with effective time management
- Critical thinking and analytical skills to understand/ analyze complex data and provide insight into risk reports, trends and outliers in data
- Computer literate and numerate with a willingness to adapt to various computer systems
Your Experience
- BSc/RN or equivalent combination of knowledge, skills and experience
- At least 3 years' experience in clinical research required
- Prior experience of Central Monitoring and associated ICH/Regulatory guidance required
- Demonstrates critical thinking skills to determine the cause and appropriate solution in the identification of issues.
- Demonstrated capability of working in global environment
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
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. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law
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