Clinical Scientist

ICON plc • Montreal, QC

10d • Remote

About The Position

ICON plc is a world-leading healthcare intelligence and clinical research organization. They are proud to foster an inclusive environment driving innovation and excellence, and welcome individuals to join their mission to shape the future of clinical development. The Clinical Scientist will assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies, which may include adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management. This role may support a single study or multiple studies, and may also lead a study with limited scope, such as a Survival Follow-up. The Clinical Scientist will interact with internal and external stakeholders, including study sites and committees, to support clinical study objectives. ICON is an award-winning workplace that enables employees to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines and medical devices. The company is also dedicated to conducting business more sustainably and supporting the communities in which they live.

Requirements

• BS/BA/MS/PhD in Life Sciences with 2+ yrs relevant career experience
• If no degree in Life Sciences, must have significant experience in clinical development (>5 years)
• At least 1 year of medical monitoring required
• Demonstrated oral and written communication skills
• Excel and PP experience required
• Ability to travel up to 15% (might include international travel)
• Legally authorized to work in the United States and/or Canada
• Should not require, now or in the future, sponsorship for employment visa status

Nice To Haves

• Pharmaceutical experience beneficial
• Experience in respiratory (specifically COPD and pulmonary Hypertension highly preferred)
• 2 years medical monitoring experience highly preferred
• ePro experience a plus

Responsibilities

• Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management
• May support a single study or multiple studies
• May lead a study with limited scope (e.g., Survival Follow-up)
• May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Benefits

• Competitive salary
• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees