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

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)
Minimum Years of Experience
Pharmaceutical experience beneficial but not required
Experience in Oncology required
2 years medical monitoring experience highly preferred
ePro experience a plus
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, and should not require, now or in the future, sponsorship for employment visa status.

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.

Clinical Scientist – Oncology

Key skills