Job Description:
• 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
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)
• Minimum Years of Experience
• Pharmaceutical experience beneficial but not required
• Experience in Oncology, ID/Vac, Neuro, Cardio, and/or Immunology 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)
• To qualify, applicants must be 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.
Benefits:
• 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.