Job Description
- 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.
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