About this role
Role Overview
- Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies
- Liaises with cross-functional lines as appropriate
- Completes timesheets accurately as required
- Updates CV as required
Requirements
- 2 years medical monitoring experience preferred
- Oncology experience is required
- Bachelor's/Masters/PhD in Life Sciences with 2+ years relevant career experience
- Proficient in written and spoken English
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development