Clinical Trials Associate Remote

Location: Quebec

## Clinical Trials Associate - Canada - Remote Apply remote type:
Remote locations:
Ontario, Canada:
Quebec, Canada time type:
Full time posted on:
Posted Yesterday job requisition :
JR102124
** 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 Trial Associate does at Worldwide
** As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.
** What you will do
*** Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
* Maintain and quality audit to assure the most recent revisions of documents are on project portals
* Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
* Maintain version and quality control of project documentation and submit to trial master file
* Assist with the tracking and maintenance of project related information, including site medical question and answer log
** What you will bring to the role
*** Excellent written and verbal English as well as fluency of the language of the country of location
* Ability to handle multiple tasks and exercise independent judgment
* Strong attention to detail and focus on quality of work
* Strong organizational and problem-solving skills
* Excellent skills in MS Office applications including Outlook, Word, Excel and Power Point
** Your experience
*** Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
* Skill sets and proven performance equivalent to the above

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 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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