Sr. CTM
Planet Pharma · Waltham, MA · 2 mo ago
OTHRContract
About the role
This person will be working closely with the Phase II/III study leaders. They need to have global phase II/III experience.
Responsibilities
- Work closely with Phase II/III study leaders
- Determine how work will be divided among the team at the site feasibility stage
- Manage a region (EU, APAC, etc.) when assigned
- Manage vendors to contracts effectively
- Handle multiple tasks and projects effectively
- Manage multiple project budgets with increasing complexity and value
- Ensure quality in all managed activities
- Use knowledge of SharePoint and Smartsheets
Requirements
- Bachelor’s Degree
- Detailed understanding of clinical trial process across all phases and ICH GCP
- Ability to understand clinical protocols and associated study specifications
- Detailed understanding and proven experience with site start-up processes
- Strong organizational skills
- Strong written and verbal communication and interpersonal skills
- Quality-driven in all managed activities