Senior Clinical Research Associate Remote

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 the Clinical Operations Department does at Worldwide Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial.

All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience - one you can’t get anywhere else, with a team unlike anyone else. 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 trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.
What you will do   Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits.
Provide mentoring and guidance to less experienced CRAs and site staff when needed.
Document site visit findings via written reports.
Assess, monitor, and train study site staff on protocol adherence as required.
Review study subject safety information and informed consent.
Conduct source document verification for compliance, patient safety, and veracity of data.
Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
Ensure site compliance with IP receipt, accountability and return or destruction.
Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.
What you will bring to the role   Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to details
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS and EDC Systems
Your experience   5+ years of experience as a Clinical Research Associate
4-year university degree or RN/BSN in Nursing
Willingness to travel required
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  or connect with us on Linked In.
Worldwide is an equal opportunity…