FAQs
Is this position fully remote?
Yes, this position is remote, but it involves monitoring US trials only.
What qualifications are required for this role?
Applicants must have a minimum of a B.S., R.N., or equivalent degree, preferably in Biological Sciences.
How many years of experience in clinical trials is required?
A minimum of 2-3 years of experience in monitoring pharmaceutical industry clinical trials is required.
Is experience in Oncology trials necessary?
Yes, a minimum of 1-3 years of experience monitoring Oncology trials is necessary.
What skills are preferred for this position?
Preferred skills include analytical/risk-based monitoring experience, strong communication and influencing skills, and the ability to operate various systems and databases.
Is there a requirement for authorization to work in Canada?
Yes, applicants must be legally authorized to work in Canada and should not require sponsorship for employment visa status.
What benefits does ICON offer to its employees?
ICON offers a range of benefits, including various annual leave entitlements, health insurance options, competitive retirement planning, life assurance, and flexible optional benefits.
Are there opportunities for career advancement in this role?
Yes, opportunities for mentoring junior team members and taking on leadership roles are available.
Is diversity and inclusion valued at ICON?
Yes, diversity, inclusion, and belonging are fundamental to ICON's culture and values.
What should I do if I need reasonable accommodations during the application process?
If you need reasonable accommodations due to a medical condition or disability, please let ICON know through the specified form in the job posting.