Senior Clinical Research Associate - Oncology - Ontario

Worldwide Clinical Trials • Oakville, ON

8d • Remote

About The Position

We are Worldwide Clinical Trials, a global, midsize CRO that pushes boundaries and innovates to find cures for persistent diseases. Our mission is to work with passion and purpose every day to improve lives. In Clinical Operations, your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will work alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration is ingrained in our culture. We offer extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Through regular touchpoints and coaching conversations with your Line Manager, we ensure your professional development is a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and overcoming obstacles to make a difference in patients' lives. Experience a world of difference with us at Worldwide!

Requirements

• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to detail
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS, and EDC Systems
• 5+ years of experience as a Clinical Research Associate
• 4-year university degree OR Nursing Degree
• Experience in Oncology is required
• Candidates must reside in Canada
• Willingness to travel regionally required

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up 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 safety-related 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, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

Benefits

• 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.
• We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Associate degree