Data Management Clinical Coding Specialist - UK - Remote

at  Worldwide Clinical Trials

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.

YOUR EXPERIENCE

• Educated to degree level (preferably Life Science), Nursing qualification, or relevant industry experience
• Trained/experienced in coding with industry standard dictionaries (e.g., MedDRA, WHO-DD)
  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

WHAT YOU WILL DO

• As a priority, perform clinical coding of study data for multiple projects.
• Work closely with study teams and sponsors to establish coding procedures, implement applicable dictionaries and coding guidelines for projects as documented within the Data Management Plan.
• Generate coding consistency reports for internal Medical Monitor / peer review and for sponsor review at periodic time points specified for the project.
• Coordinate dictionary implementation and version updates for projects as applicable.
• Attend sponsor and team meeting as necessary.
• Provide regular updates to management regarding coding deliverables, metrics, coding issues, etc. as necessary.
• Ensure clinical coding operations are conducted according to Worldwide’s SOP’s.

WHAT YOU WILL BRING TO THE ROLE

• Leadership/mentorship to support junior staff performing coding activities.
• Computer literacy and numerate with a willingness to adapt to various computer systems.
• It is essential that the job holder works with close attention to detail and to be questioning about the validity of the data being entered.
• Excellent time management and man management skills.Experience within Data Management and coding of study data terminology.