Clinical Research Associate - Quebec City, Canada - Worldwide Clinical Trials

Worldwide Clinical Trials

Verified Company

Quebec City, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Requisition Number

7247

Employment Type:

Regular
Who we are

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality.

Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

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 Clinical Operations Site Management 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

Join our Neuroscience team, who provides expertise in Alzheimer's Disease & Dementia, Neurology, Pain, Psychiatry and Psychedelics
Responsible for managing the research activities at sites participating in Worldwide's clinical research projects, which are predominantly registries and other types of noninterventional / observational studies
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study startup activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safetyrelated events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
Conduct study initiation visits (SIVs)
While most of the site management efforts will be performed remotely, will be required to ensure compliance with obtaining informed consent, reporting potential safetyrelated events, and adhering to all applicable regulatory requirements

What you will bring to the role