Assists the SM Study Lead and study team with the operational conduct of clinical studies (e.g., CTT minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities)
May support a single study or multiple studies
May lead a study with limited scope (e.g., Survival Follow-up)
May be responsible for tracking study timelines and will be proficient in project management tools
May interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectives

BS/BA/MS/PhD with 2+ yrs clinical research experience
Pharmaceutical and/or clinical drug development experience beneficial but not required
Oncology TA experience required (trial management)
Demonstrated oral and written communication skills
Excel and PP experience required
Legally authorized to work in the United States 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.

Study Manager – Oncology

Key skills