This is a brand new unblended CRA opportunity to work dedicated to a top 5 pharmaceutical company worldwide.
We are looking for a junior CRA based in Madrid
- The uCRA is responsible for ensuring accurate pharmacy documentation is in place, investigational medicinal product (IMP) accountability is maintained and blinded and unblinded site staff members can work in a coordinated manner without compromising the blind.
- The uCRAs will ensure that IMP supplies are maintained in suitable storage conditions and are accurately reconstituted, dispensed, administered, returned and destroyed.
- All appropriate documentation will be maintained and a study drug re-supply procedure will be put in place where necessary.
Life Science educational background
Master´s Degree in Clinical monitoring
Fluent English levelExperience:
At least 6 months of monitoring experience.
Apply on company website