What are the responsibilities and job description for the Clinical Trial Administrator position at ProPharma Group?
At ProPharma Group, we have improved the health and wellness of patients for 20 years by empowering biotech, med device, and pharmaceutical organizations to confidently advance scientific breakthroughs and introduce new therapies.
Key Responsibilities
- Administer all contract management processes from start of document draft, through final document completion, negotiations, agreement, and signatures.
- Support agreement on country template contract and budget.
- Negotiate budgets and contracts with sites and cross-functional teams.
- Lead quality control and arrange execution of CTAs, archival of documents into repositories, and capture of metadata.
