Central Monitor - US/Canada - Home-based

Location: North Carolina, USA

Notice

This position is no longer open.

Requisition Number: 6184

Position Title: Central Monitor

External Description:

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 3000 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 you will do

  • Understands the assigned protocol and ensures central monitoring activities are planned and executed in alignment with it and in adherence to ICH-GCP, SOPs, corporate standards and regulatory requirements.  
  • 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.
  • As required, develops and delivers training to the study team regarding the centralized monitoring strategy.
  • Can provide subject matter expertise for the delivery of the centralized monitoring strategy required for the trial. Ensures the documentation of the centralized monitoring strategy in the appropriate functional plan and/or development of the central monitoring plan. 

 

What you will bring to the role

 

  • Knowledge of clinical project financial principles
  • Ability to apply problem solving techniques to resolve complex issues and apply a risk management approach to identify and mitigate potential threats to the successful conduct of a clinical research project.
  • 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 background

 

  • 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

 

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! 

 

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Employment Type: Regular

Community / Marketing Title: Central Monitor - US/Canada - Home-based

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

Location_formattedLocationLong: North Carolina, US

CountryEEOText_Description: 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 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. Worldwide is committed to working with and providing reasonable accommodations to applicants with disabilities. We are proud to be an equal opportunity workplace where people thrive by being themselves and are inspired to do their best work every day.

 Worldwide Clinical Trials does not accept unsolicited resumes from 3rd party vendors

© Worldwide Clinical Trials 2023

We only accept resumes from staffing organizations with pre-approved contractual agreements. Please do not forward resumes directly to our hiring managers, jobs alias, or any other company location. Unsolicited resumes from employment agencies will not be considered and Worldwide is not responsible for any fees related to unsolicited resumes.