Offer summary
Qualifications:
University degree in life sciences/pharmacy, Two years experience as a CRA, Experience in clinical research site management, Fluency in English and local language if applicable, Ability to travel up to 60%.
Key responsabilities:
- Manage study site activities and patient safety
- Conduct site visits, monitor compliance with protocols
- Maintain study trial management tools and report status
- Assist with start-up procedures and contract negotiations
- Document and communicate site progress and risks